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40 Jobs Found 

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Packaging Engineer

Elanco

Liverpool, Liverpool
18 days ago
Liverpool, Liverpool
18 days ago

Interested in joining a cause-driven, customer focused company dedicated to positively impacting the health of animals, people and the planet? Search our job listings below.


This position will support the packaging of Elanco products at Elanco Contract Manufacturing sites within EMEA & APAC. This position will have direct responsibility for key Elanco packaging projects and will provide technical oversight to ensure Elanco products are packaged in a safe, efficient, and compliant manner.

Key Objectives/Deliverables:

  • Knowledgeable of packaging materials and packaging equipment for multiple platforms (blister, bottle, syringe, vial, cartons, etc.)
  • Ability to evaluate existing packaging formats and packaging operations to improve productivity and initiate cost savings projects.
  • Originate change controls and events to support packaging material changes that effect operations at Contract Manufactures (CMs) and Elanco sites as needed.
  • Understand the packaging requirements for international shipments, including dangerous goods and UN certification.
  • Interface with internal teams and external suppliers to conduct packaging testing (including shipping validations) of packaging materials and packaged components.
  • Support the process qualification and validation of packaging equipment on key projects that evaluates the new or modified packaging components at CMs and internal Elanco sites.
  • Provide guidance regarding technical protocols and reports for primary, secondary and tertiary packaging components and associated qualifications and/or validations.
  • Experience with process qualification and validation across various packaging technologies within pharmaceutical packaging formats (blisters, bottles, bags, sachets, cartons, form fill seal, parenteral, etc.)
  • Accountable for updating and maintaining packaging specifications as required to support packaging operations at CMs.  This would include primary, secondary and tertiary packaging components, ensuring that all Elanco products are compliant with RCD (Regulatory Commitment Documents).
  • Author, review and approve packaging instructions as applicable, generated by CMOs or Elanco internal sites to perform packaging of Elanco products.
  • Awareness of industry and regulatory developments with respect to packaging materials.
  • Support the packaging artwork change process by providing the appropriate dimensional templates for packaging components (cartons, labels, bags, etc.) that allows the art studio to layout the text and graphics properly on the packaging component. 
  • Provide guidance around the design and selection of primary, secondary and tertiary packaging components and suppliers.
  • Support the Audit group in auditing of Packaging manufacturers and suppliers.
  • Technical representative for packaging deviations and ensures deviations and complaints are investigated thoroughly to ensure that a corrective action is consistent with the root cause analysis.

Basic Requirements:

  • Strong problem solving capabilities including strategic and creative thinking
  • Strong interpersonal/communication skill: verbal and written
  • Excellent project management skills - ability to support projects with contract manufacturing organizations
  • Cross-functional networking and influencing ability
  • Ability to handle multiple priorities and deal with ambiguity
  • Good understanding of packaging equipment, materials, and technologies utilized in the pharmaceutical industry.
  • Thorough understanding of cGMP regulations and regulatory agencies packaging requirements from (country relevant Pharmacopeias)
  • Must have experience in working with equipment vendors and distributors, for packaging engineering projects and support activities.
  • Self-motivated Demonstrated strong documentation skills.
  • Demonstrated strong oral and written communication and interpersonal interaction skills.

Education/Experience

  • Bachelor’s Degree or Diploma (or equivalent work experience)
  • 5+ years prior Packaging Experience
  • Ability to prioritize multiple activities
  • Ability to influence others

Languages

  • English: fluent spoken and written. German & French as an advantage

  • Reports to: EEM EMEA Hub Leader

Site

  • Multiple Locations

 Travel

  • This position serves an 8-hour Monday through Friday work schedule
  • Situations may arise where off-schedule work, both on-site and off-site may be required
  • This position may require 30-35% travel to contract manufacturing and Elanco manufacturing sites, domestic and international locations on an annual basis

Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status

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Manufacturing Manager

Applicant Services

Manchester, NW
Today
Manchester, NW
£42k - £43k Per Year
Today
£42k - £43k Per Year

This could be your chance to work for a nationwide respected Heat Treatment company! Established in 1974, our client is one of the UK's leading Heat Treatment engineering companies. 

MANUFACTURING MANAGER (Heat Treatment Systems)

£42,500 per annum + 25 days paid annual leave

This progressive heat treatment equipment manufacturing company are looking to recruit a Manufacturing Manager for their Wigan works.

The successful candidate will be based out of our office in Wigan, working Monday to Friday 08:00 - 17:00hrs. Primary day to day duties of this role will include but not be limited to:

Primary day to day duties of this role will include but not be limited to:

  • Daily management of the manufacturing employee’s workload, currently a team of six.
  • Purchase order processing.
  • Sales order processing.
  • Overlooking stock control.
  • Liaising with shipping companies with regards to importing and exporting of goods.
  • Setting up of new products on our system.
  • Setting up and maintaining bills of materials.
  • Dealing with customer enquiries.
  • Dealing with supplier enquiries.
  • Reading engineering drawings.
  • Creating engineering drawings.
  • Maintaining and keeping up to date the training records relating to the manufacturing employees.
  • Collating the weekly hours and forwarding this information to payroll to enable the weekly wages to be processed.

About you

The ideal candidate will be from an engineering background and preference will be given to applications that demonstrate experience of AutoCAD and Sage 200.

You will also need to demonstrate effective leadership skills coupled with excellent time management and organisation ability.

How to apply for the Manufacturing Manager job

Click “apply” for your new career now! Watch out for an email giving you more information on how to tailor your application and provide a cover letter or any other supporting documents you may have.

You must be eligible to work in the UK

Suitable skills and experience include production manager, production leader, manufacturing leader, mechanical engineering management, engineering manager, heating and mechanical manager, thermal engineer manager.

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Manufacturing Manager

Professional

Stretford, NW
1 day ago
Stretford, NW
£35k - £45k Per Year
1 day ago
£35k - £45k Per Year

Manufacturing Manager
£35,000 to £45,000 depending on experience
Trafford Park
Permanent
Manufacturing Manager
The Candidate
You will be an experienced Manufacturing Manager / Production Manager / Operations Manager who has experience of working in a world class manufacturing environment. With a strong knowledge in lean and six sigma you will also have the following skills, experience and attributes…
⦁ A strong Health and Safety mentality with an IOSH / NEBOSH qualification.
⦁ At least 5 years’ experience leading a multi shift team.
⦁ Must have experience of multi department management
⦁ Knowledge of printing technology ideal but not essential.
⦁ Evidence of success coaching / mentoring team members.
⦁ Ideally you will have a knowledge of Six Sigma and have earned a yellow or green belt
⦁ Compliant in CI methodologies, and able to deliver strategic data evidence to board level.
⦁ The ability to work to targets and achieve KPI’s
⦁ Able to manage, motivate and lead a team to achieve targets
⦁ Excellent prioritisation skills and able to juggle competing demands
⦁ Must have a can-do attitude, welcome a challenge, and approach hard work with a positive outlook.
⦁ Excellent customer focus and commitment to ensuring customer satisfaction
⦁ Attention to detail
⦁ Computer literate: knowledge of Microsoft office
⦁ Able to remain calm under pressure
⦁ Good problem-solving skills
The Role
You will be responsible for 4 direct reports and 70 indirect reports across 3 shifts and 3 different production departments. The company operates in a modern manufacturing environment with state-of-the-art machinery and is well on the way in their lean manufacturing journey. Your role will be to facilitate this journey embracing a culture of continuous improvement while mentoring, developing and leading the team. Your main responsibilities will include…
This will involve using your world class manufacturing knowledge to ensure all operational targets for H&S, Quality, Cost, Service and employee engagement are achieved and continually improved.
⦁ Maintain a safe and legal working environment – lead role for H&S compliance.
⦁ Delivery of KPIs focussing on Health & Safety, Quality, Cost and Service. This will include machine efficiency, error rate and meeting customer SLAs
⦁ Continually improve systems and processes to reduce the lead-time to our customers.
⦁ Continually improve the quality to enhance the customer experience.
⦁ Manage, as part of a team, the maintenance of the equipment to maximise uptime.
⦁ Lead and motivate the Team Leader group to achieve and exceed their departmental goals.
⦁ Contribute to the employee engagement and cultural journey by living the core values.
⦁ Identify capacity issues and suggest investment options.
⦁ Liaise with HR to plan and execute excellent recruitment, training and development for all team members.
⦁ Liaise with Finance to monitor departmental spend and ensure value for money is achieved.
⦁ Be part of the out of hours response team.
⦁ Take ownership of product manufacture, from cradle to grave, with a right first time, every time attitude.
⦁ Be the pinnacle in cultural improvement and be key to the overall improvement of the business.
⦁ Stay at the forefront of technology developments within the garment decoration industry
The Company
Our client is a market leader and is experiencing year on year growth of around 20%. An opportunity has arisen for an experienced Manufacturing Manager to join the business and help to deliver and be part of this growth.


The UK has now left the European Union. Any EU, EEA or Swiss citizens living in the UK that wish to remain in the UK post Brexit need to apply to the EU Settlement Scheme. Please visit our resource section on our website for more information.

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Supplier Quality Engineer / Manufacturing

AWD online

Leyland, NW
Today
Leyland, NW
£40k - £45k Per Year
Today
£40k - £45k Per Year

Supplier Quality Engineer who has good working knowledge of supplier process management and controls, PPAP, APQP and supporting programmes is required for a well-established company based in Leyland, Lancashire, North West England.

 

 

SALARY: £40,000 - £45,000 + Excellent Benefits (25 Days Holiday, plus 8 Statutory Bank Holidays, Pension Scheme, Private Outpatients Scheme)

 

LOCATION: Leyland, Lancashire, North West England       

 

JOB TYPE: Full-Time, Permanent

 

 

PLEASE NOTE: This is a “Field-Based” role with the potential for extensive travel both within & outside of the UK.

 

 

JOB OVERVIEW

 

We have a fantastic new job opportunity for a Supplier Quality Engineer who has good working knowledge of supplier process management and controls, PPAP, APQP and supporting programmes.

 

Working as the Supplier Quality Engineer your duties and responsibilities will include:

 

  • Initiate APQP (Advanced Product Quality Planning) multi-functional teams

 

  • Co-ordinate PPAP (Production Part Approval Process) activities at the supplier and manage into plant

 

  • Initiate supplier / launch readiness reviews and quality plans

 

  • Facilitate, prioritise, train and support supplier corrective action meetings and reviews

 

  • Measure and analyse trends and performance at the supplier and the plant to reduce potential issues

 

  • Develop the supplier base by using Six Sigma and Lean techniques

 

  • Liaise with the Group to develop integration activities with the supply base

 

  • Analyse and audit processes and parts at suppliers premises

 

  • Complete root cause analysis programmes to plant satisfaction

 

  • Be business aware and predict industry trends

 

 

CANDIDATE REQUIREMENTS

 

As the Supplier Quality Engineer you will have the following skills, experience and attributes:

 

  • Working knowledge of supplier process management and controls, PPAP, APQP, and supporting programmes

 

  • Experience undertaking measurement system analysis, statistical measurement and trend analysis (MSA, SPC & PFMEA).

 

  • Internal and external experience in auditing systems and capabilities or possess a qualification in such systems

 

  • Capable of effective decision making

 

  • Skilled / experienced in root cause analysis and poka yoke

 

  • Confident to discuss, enforce and recommend any concerns, solutions and constraints at the highest level

 

  • Degree qualified or studying towards a degree

 

  • Six Sigma certification desirable

 

  • Possess excellent presentation skills, and the ability to see tasks through to a logical conclusion

 

  • PC literate

 

  • Willing to travel on a regular basis and prepared to spend time away from home

 

 

HOW TO APPLY

 

To be considered for this job vacancy, please submit your CV to our Recruitment Team who will review your details. CV’s of Job Applicants meeting this requirement will be submitted to our Client for consideration. By submitting your job application to us you are hereby giving us your express consent to submit your details to our Client for this purpose.

 

JOB REF:AWDO-P6127

 

Full-Time, Permanent Supplier Quality Engineer Jobs, Careers and Vacancies. Find a new job and work in Leyland, Lancashire, North West England. Multi-Job Board Advertising and CV Sourcing Recruitment Services provided by AWD online.

 

AWD online operates as an employment agency

 

awdonline | http://www.awdo.co.uk

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Electrical Manufacturing Manager

Cameron Clarke Associates t/a talent-finder

Widnes, NW
2 days ago
Widnes, NW
£32k - £32k Per Year
2 days ago
£32k - £32k Per Year

Control Panel Manufacturing Manager

An exciting position has become available for a full time Control Panel Manufacturing Manager to join a friendly team based in Widnes. The successful candidate will earn £32,000 upwards depending on experience. Ideally the applicant must have good experience within the control panel industry and have technical ability to communicate with engineers and project managers. The applicant would benefit from having electrical & mechanical knowledge.

Role Requirements

•Strong management skills
•Ability to understand electrical schematic drawings
•Planning labour with assistance from the projects team
•Good communication skills
•Ability to identify drawing problems
•Problem solving & Strong decision making
•Customer facing
•Commercial awareness against projects

Role Responsibilities

•Having overall accountability for the safety of the employees working within the manufacturing areas.
•Being accountable for manufacturing process quality; managing adherence to quality standards and procedures.
•Holding accountability for achieving customer delivery and manufacturing schedule adherence targets including implementation of continuous improvement strategies.
•Analysing and interpreting data to identify opportunities to improve efficiency and effectiveness of production output.
•Leading, developing, and motivating staff members

Company

Our client is a Cheshire based Technical Controls & Automation company.

They are a busy technical automation company who specialise within a wide range of sectors but not limited to: - Automotive, Pharmacy, Oil & Gas, food & Beverage and Chemical.

All projects are designed inhouse and are bespoke to each customer’s needs.

Why should you apply?

•To join a fantastic company
•To become part of a great team
•To showcase your knowledge and skill set

If you’re the ideal candidate our client is looking for, please send your CV by clicking the APPLY button

Keywords: Control Panel, Manufacturing Manager, Management, Panel, Technicians, Workshop, Electrical Schematic Drawings, Drawing, Bespoke

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Quality Engineer / Manufacturing

AWD online

Bolton, NW
Today
Bolton, NW
Today

Quality Engineer who has previous experience working within a Quality Function, including carrying out FMEA’s and 8D is required for a well-established International Company based in Westhoughton, Bolton, Greater Manchester.

 

 

SALARY: Excellent Package 

 

LOCATION: Westhoughton, Bolton, Greater Manchester    

 

JOB TYPE: Full-Time, Permanent

 

 

APPLICATION PROCESS: Candidates will be required to complete an online application form and the details will be emailed over separately. Please keep an eye out for our email.

 

 

JOB OVERVIEW

 

We have a fantastic new job opportunity for a Quality Engineer who has previous experience working within a Quality Function, including carrying out FMEA’s and 8D.

 

Working as the Quality Engineer you will:

 

  • Carry out 8D investigations for customer complaints and concerns and drive the Corrective/Preventative Actions required. Support the internal NCR/CAR process, Quarantine management and work with the relevant departments to ensure good Corrective actions are implemented

 

  • Ensure FMEA’s are carried out for all processes / products and are kept current and used for design capability evaluation and change control management. Develop Quality Control Plans for all products ensuring they are kept current; ensuring governance through SOP’s and communication to operations

 

  • Support the other members of the Technical/Quality Team

 

  • New Product Risk Assessment – representing quality at high-risk job, planning and post job review meetings

 

  • Assist in performing in-process testing of Product and associated Tooling

 

  • Support root cause analysis and corrective action for external and internal customer concerns.

 

  • Support the Quality & OpEx Manager and other members of the Quality Team

 

 

DUTIES

 

As the Quality Engineer your key responsibilities include:

 

  • Conduct investigations using 8D process for Customer complaints and generating reports that can be passed to the Customer

 

  • Support the NCR/CAR system and actively work with the relevant departments to drive the process.

 

  • Ensure that all products / processes are assessed using the FMEA process and then update the assessments on a continual basis.  Run teams to achieve this.

 

  • Develop comprehensive Quality Control Plans for all products

 

  • Gather statistical data and prepare quality reports

 

  • Maintain an effective Quarantine and segregation process for all nonconforming raw materials

 

  • Communicate and escalate urgent Quality concerns to the Quality & OpEx Manager

 

  • Ensure Corrective and Preventative Actions are implemented for external and internal issues

 

  • Use Quality Improvement tools to problem solve and continually improve the level of quality and performance

 

  • Provide daily, weekly, monthly quality reports

 

  • Be an active member of the internal Auditing team for the company’s ISO management systems

 

  • Assist in the improvement of Quality systems and SOP’s

 

  • Liaising with the Technical Process and R&D departments as required on Quality and testing process issues

 

 

CANDIDATE REQUIREMENTS

 

As the Quality Engineer you will have the following skills, experience and attributes:

 

  • Previous experience of working within a Quality function, including carrying out FMEAs and 8D

 

  • Good communication skills at all levels, both written and verbal

 

  • Experience in solving problems & driving improvements utilising data

 

  • High level of dexterity & attention to detail; good eyesight and able to discern colour

 

  • Experience of Statistical Process Control (SPC)

 

  • Skilled in the use of the full range of Quality Improvement tools

 

  • Good Leadership/People Management skills

 

  • Flexible approach to working requirements including supporting the rest of the team and covering absences.

 

  • Experience of working to tight deadlines

 

  • Work with other sites and the Central Teams when required on any required issues and projects

 

 

HOW TO APPLY

 

Once you’ve applied for this role through this site you will be required to complete an online application form and the details will be emailed over separately. Please keep an eye out for our email.

 

By submitting your job application to us you are hereby giving us your express consent to submit your details to our Client for this purpose.

 

JOB REF:AWDO-P6072

 

Full-Time, Permanent Jobs, Careers and Vacancies. Find a new job and work in Westhoughton, Bolton, Greater Manchester. Multi-Job Board Advertising and CV Sourcing Recruitment Services provided by AWD online.

 

AWD online operates as an employment agency

 

awdonline | http://www.awdo.co.uk

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Supplier Quality Engineer (12 month FTC) - Manchester, England, UK

Hologic

Manchester
7 days ago
Manchester
7 days ago
Hologic is the market leader in the women’s health industry with three different divisions, all offering unparalleled diagnostic and treatment solutions. In the regulated markets where businesses are awarded on a tender basis, our capability to win the deal comes from seamless combination of Customer solution definition (Commercial and Technical content) together with flawless execution of all tender requirements (Administrative content and process).
JOB SUMMARY
This position provides support to the Global Supplier Quality organization dedicated to the oversight of Chem/Bio/Packaging components/subassemblies. He/she will provide technical knowledge across the organization to ensure suppliers can meet all requirements.
Internally interacts with :
+ Sites having quality raw material problems.
+ Post Market Surveillance around raw materials situations.
+ R and D sustaining on raw materials specification changes.
+ Other Hologic Departments, such as Procurement, Product Quality, Quality Assurance, Supply Chain, Manufacturing Engineering, Design Engineering (Research and Development), among others.
Externally interacts with:
+ Current and potential new suppliers of raw materials around the world.
ROLE ESSENTIAL DUTIES AND RESPONSIBILITIES
+ Execute all applicable activities to comply with regulatory standards and meet the requirements stablished in the Quality Management System around supplier’s quality management.
+ Coordinate and execute activities related to the implementation of new raw material suppliers as a result of the introduction of new products, transfer of products, alternate suppliers, etc.; ensuring that the suppliers comply with the requirements stipulated in the quality system before the closure of the projects.
+ Conduct technical reviews on raw material suppliers to understand their capability to make parts/raw materials.
+ Oversee, asses and monitor suppliers making parts as it relates to manufacturing, process and quality control practices, corrective action, continuous improvement, and “First Article Inspection”.
+ Follow PPAP (Production Part Approval Process) requirement for all new and revised purchased parts (as applicable). Follow up for their on-time completion.
+ Work collaboratively with raw material suppliers on problem solving and root cause analysis to avoid failures. Apply (as applicable), metrology and statistical measurement to problem analysis and resolution.
+ Work with Post Market Surveillance and other applicable departments (Quality Engineering, MFG Engineering, Research and Development, etc.) to understand complaints linked to raw material situations.
+ Maintain complete supplier quality records as per the applicable procedure (e.g., supplier performance key indicators, supplier’s quality certifications, etc.). Update raw material suppliers’ files when required and check that the information is accurate and complete, assuring that all applicable regulatory standards are met.
+ Update the ERP system with the status of the approved suppliers for the different raw materials.
+ Resolve quality day to day issues associated with raw material suppliers around the globe by addressing non-conformities: call into containment and work along with the corresponding departments to achieve disposition of the impacted raw material (return to supplier, rework, sort, etc.). If applicable, collect and send back samples to suppliers if needed.
+ Support audits, where applicable, as a subject matter expert in Chem/Bio/Packaging components/subassemblies. Travel might be required.
+ As applicable, attend to functional and departmental meetings as Supplier Quality representative and follow up on action items accordingly.
+ If needed, coordinate/execute the change in specifications and/or procedures when required through the corresponding change order.
+ Train in the respective procedures in the training system, before executing the respective task.
+ Maintain supplier performance metrics to be used in decision making. Provide the necessary reports to other departments as required.
+ Note: The focus of this position will be Chemical/Biological/Packaging suppliers, however, per management discretion, he/she might be required to perform other duties linked to supplier quality.
QUALIFICATIONS
+ Working knowledge of ISO 13485 and 21 CFR part 820
+ QMS/ISO 9001 or 13485 Lead Auditor Training / Internal Auditor Training
+ Full Clean Driving licence.
EDUCATION AND EXPERIENCE
+ 3-5+ years’ experience in IVD or medical device manufacturing or related industry
+ Demonstrated practical approach towards decision making and problem resolution
+ Good understanding of supplier quality.
PHYSICAL DEMANDS
+ Flexible working hours and travel is required for business requirements.
WORK ENVIRONMENT
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
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Production Manager

Restore Digital

Warrington, NW
2 days ago
Warrington, NW
2 days ago

Restore Digital is a leading independent provider of document scanning, business process automation solutions, and professional consultancy services. Our customers trust us with their business critical and highly sensitive data. We have helped NHS Trusts, Central Government, Nuclear, and Police Authorities, amongst other industries, begin their digital transformation journey and save £millions while protecting against risk.  We also offer the largest scanning capacity in Europe.  We are one of five business units of Restore plc and are rapidly expanding and looking for hardworking and enthusiastic people to join a highly successful and established team in Warrington.

 

Our Production Manager supports our Team Leaders ensuring that work is carried out to production targets, job specs, and quality standards in line with customer requirements.  They support our busy team leaders through regular coaching and guidance to ensure they are confident and competent to deliver what’s needed.  In addition to this they are the digitisation lead for the site and come to the role with a thorough understanding of the digitisation process for document scanning.  Confidentiality is a must too and our Production Manager is security cleared to the Government’s Baseline Personnel Security Standard (BPSS).  Our hours of work are 7.30am to 3.30pm Monday to Friday.

 

We offer a competitive salary along with all the training and support you will need to be a success in your new role.  In addition to the usual benefits, we also have a company benefits system which offers discounts on everything from holidays and cinema tickets, to meals out and much more. 

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Director, Primary Manufacturing

Seqirus

Liverpool
22 days ago
Liverpool
22 days ago

Come join a company that tackles fascinating problems and find solutions to complex challenges.  With deep expertise in influenza science, our team works on cutting-edge research, pioneering technologies to optimise the manufacturing process and improve the effectiveness of influenza vaccines. We operate as one integrated global organisation, drawing together expert staff from different countries to collaborate. Together, we are working on the front line to protect communities from seasonal influenza and global pandemic threats. When you join Seqirus, you join a team dedicated to making a difference in people's lives. It's a feeling of possibility, creativity, and purpose that inspires us every day.

The incumbent is accountable for leading, directing, and managing all aspects of the Primary Manufacturing business unit in Liverpool.  This includes achieving supply targets and optimizing manufacturing productivity and output for Primary Manufacturing. Management duties include directing aspects of personnel, facility, process, and equipment for a large scale manufacturing facility. This individual will serve as the leader coordinating the department for both process development and commercial material production. This individual will assume full responsibility as the department representative on key development projects.  This leader will also sit on the site leadership team and will be responsible for playing a key role in the overall leadership of the Liverpool Site.

This role has direct functional responsibility includes approximately 150 FTE staff members.

  • Directs multiple teams of manufacturing staff to ensure manufacturing in accordance with schedule / customer requirements within the agreed financial constraints and according to the relevant.

  • Accountable to achieve supply targets.

  • Ensures compliance in accordance to Seqirus’s quality, compliance, safety, GMP, and regulatory standards at all times

  • Sets department policy regarding staffing, hours and job junction to meet planned projects and production goals.

  • Responsible for ensuring the GMP requirements for facility and documentation for commercial material production. Works with QA/Compliance group for GMP certification of the facility and equipment. Writes and reviews GMP documents like Standard Operating Procedures and Batch Process Records. Works with the QA Raw Materials group in specifying the GMP materials needed for commercial material production

  • Responsible for ensuring that all staff are properly trained in their duties

  • Devises solutions for problems of complex scope which affect multiple areas within manufacturing. Develops operational processes and production protocols. Oversees the design, execution, and analysis or results from experiments to ascertain that high-quality data is generated. Plays a key role in troubleshooting problems in manufacturing operations

  • Assumes full responsibility as the department representative on capital projects. Makes conceptual contributions to project strategies and achievements. Directs manufacturing staff in the execution of capital projects

Knowledge, Skills & Competencies

Technical Skills

  • Subject matter expert in drug substance related operations including cell culture and purification technologies

  • Understand of Engineering and Automation best practices

  • Lean Manufacturing Methodologies

Building Effective Teams:

  • Creates high impact, efficient teams across the function, including members with different but complementary skills and expertise

  • Empowers team leads and managers to work together to make decisions and accomplish goals, providing mentorship and support when needed

  • Serves as an advocate for teams across the function, prioritizing demands, ensuring organizational support and resolving issues

Developing Direct Reports and Others

  • Motivates others, including senior leaders, to take responsibility and have proactive discussions about career goals and development

  • Encourages and promotes learning opportunities for employees to develop across the function, creating a safe environment for employees to demonstrate new skills

  • Advocates for employees and managers by communicating their capabilities and accomplishments across the function

  • Provides input and suggestions to other leaders within the function regarding efficient delegation and staffing decisions

  • Contributes to long-term workload planning, ensuring that leaders within the function are informed of staffing and resource needs

  • Enables a culture of ownership and delegation by giving individual authority and responsibility to senior managers and leaders

Strategic Agility

  • Accurately anticipates future consequences and trends, assessing the internal and external environment and leveraging new sources of data 

  • Communicates the vision and goals of the function to employees in a compelling manner to gain support and motivation

Identifies criteria to assess strategic alignment and success of plans, tracking against measurable success factors

Minimum Experience Requirements

  • Minimum 10+ years’ related industry experience required

  • At least 7 years of production management experience preferred

  • Demonstrated knowledge of GMPs and FDA requirements

  • Strong demonstrated team leadership skills

  • Strong project management skills preferred

  • Manufacturing Financial Knowledge – understanding of manufacturing financial accounting (budgeting, bills of materials, variances, recoveries, depreciation, working capital, etc.) and analytical skills to identify problems and opportunities.

  • Continuous improvement orientation.

  • Ability to lead change. 

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Site Production Manager

Professional

Manchester, NW
5 days ago
Manchester, NW
£30k - £35k Per Year
5 days ago
£30k - £35k Per Year

Site Production Manager
Circa £30-35,000 per annum
Monday to Friday 8am to 5.30pm
Manchester
The Candidate

• Experience as a Site Manager, Operations Manager, Production Manager or similar is essential.
• Experience of production / manufacturing, ideally in a waste / recycling / chemicals etc would be ideal. Fast moving environment is vital.
• Any experience with transport / logistics would be advantageous.
• Strong man-management skills are key
• Able to work in a fast paced, demanding environment.
• Excellent communication skills.
• Strong SHEQ experience.
The Role

You will be responsible for managing the Production and Logistics function of a busy site. Duties will include...
• Staff management including training and development as well as managing staffing levels.
• Ensure Quality is in line with expectations and customer requirement.
• Produce monthly production report and site traffic plan.
• Ensure machinery is in working order and investigate any damages to the site or equipment.
• Complete daily walk-around checks to ensure site is running as expected.
• KPI management.
• Ensure trailers are all loaded in a timely manner.
• Planning of supplies and deliveries to ensure there is adequate stock
• Overall site housekeeping at an agreed standard
• Responsibility for SHEQ across the site.
The Company
Our client is seeking a Site Manager to join its growing team. They are a leading business in their industry and this role represents an exciting opportunity to help the firm grow and develop.
Proman acts as an employment agency for permanent staff and an employment business for temporary workers. We recruit for roles based in Engineering, Technical, Warehousing, Manufacturing, Office, Logistics and Industrial.
View our latest jobs today on our website www.proman-uk.com and follow us on LinkedIn.
APPH


The UK has now left the European Union. Any EU, EEA or Swiss citizens living in the UK that wish to remain in the UK post Brexit need to apply to the EU Settlement Scheme. Please visit our resource section on our website for more information.

Posted

18 days ago

Description

Interested in joining a cause-driven, customer focused company dedicated to positively impacting the health of animals, people and the planet? Search our job listings below.


 

This position will support the packaging of Elanco products at Elanco Contract Manufacturing sites within EMEA & APAC. This position will have direct responsibility for key Elanco packaging projects and will provide technical oversight to ensure Elanco products are packaged in a safe, efficient, and compliant manner.

Key Objectives/Deliverables:

  • Knowledgeable of packaging materials and packaging equipment for multiple platforms (blister, bottle, syringe, vial, cartons, etc.)
  • Ability to evaluate existing packaging formats and packaging operations to improve productivity and initiate cost savings projects.
  • Originate change controls and events to support packaging material changes that effect operations at Contract Manufactures (CMs) and Elanco sites as needed.
  • Understand the packaging requirements for international shipments, including dangerous goods and UN certification.
  • Interface with internal teams and external suppliers to conduct packaging testing (including shipping validations) of packaging materials and packaged components.
  • Support the process qualification and validation of packaging equipment on key projects that evaluates the new or modified packaging components at CMs and internal Elanco sites.
  • Provide guidance regarding technical protocols and reports for primary, secondary and tertiary packaging components and associated qualifications and/or validations.
  • Experience with process qualification and validation across various packaging technologies within pharmaceutical packaging formats (blisters, bottles, bags, sachets, cartons, form fill seal, parenteral, etc.)
  • Accountable for updating and maintaining packaging specifications as required to support packaging operations at CMs.  This would include primary, secondary and tertiary packaging components, ensuring that all Elanco products are compliant with RCD (Regulatory Commitment Documents).
  • Author, review and approve packaging instructions as applicable, generated by CMOs or Elanco internal sites to perform packaging of Elanco products.
  • Awareness of industry and regulatory developments with respect to packaging materials.
  • Support the packaging artwork change process by providing the appropriate dimensional templates for packaging components (cartons, labels, bags, etc.) that allows the art studio to layout the text and graphics properly on the packaging component. 
  • Provide guidance around the design and selection of primary, secondary and tertiary packaging components and suppliers.
  • Support the Audit group in auditing of Packaging manufacturers and suppliers.
  • Technical representative for packaging deviations and ensures deviations and complaints are investigated thoroughly to ensure that a corrective action is consistent with the root cause analysis.

Basic Requirements:

  • Strong problem solving capabilities including strategic and creative thinking
  • Strong interpersonal/communication skill: verbal and written
  • Excellent project management skills - ability to support projects with contract manufacturing organizations
  • Cross-functional networking and influencing ability
  • Ability to handle multiple priorities and deal with ambiguity
  • Good understanding of packaging equipment, materials, and technologies utilized in the pharmaceutical industry.
  • Thorough understanding of cGMP regulations and regulatory agencies packaging requirements from (country relevant Pharmacopeias)
  • Must have experience in working with equipment vendors and distributors, for packaging engineering projects and support activities.
  • Self-motivated Demonstrated strong documentation skills.
  • Demonstrated strong oral and written communication and interpersonal interaction skills.

Education/Experience

  • Bachelor’s Degree or Diploma (or equivalent work experience)
  • 5+ years prior Packaging Experience
  • Ability to prioritize multiple activities
  • Ability to influence others

Languages

  • English: fluent spoken and written. German & French as an advantage

  • Reports to: EEM EMEA Hub Leader

Site

  • Multiple Locations

 Travel

  • This position serves an 8-hour Monday through Friday work schedule
  • Situations may arise where off-schedule work, both on-site and off-site may be required
  • This position may require 30-35% travel to contract manufacturing and Elanco manufacturing sites, domestic and international locations on an annual basis

Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status

Source: Elanco