Wockhardt's Current Vacancies

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Senior Regulatory Affairs Executive details

Senior Regulatory Affairs Executive

Senior Regulatory Affairs Executive

Contract:

Permanent/full-time]

Deadline:

20th February 2020

 

Are you an experienced Regulatory professional looking for the next step in your career? Do you enjoy working in a fast-paced environment where you can utilise your expertise, strategic thinking and problem-solving skills? Would you like to participate in a range of interesting and complex projects, including new marketing authorisation applications?

Then look no further! A fantastic opportunity has arisen for a Senior Regulatory Affairs Executive to join one of the largest generic pharmaceutical companies in the UK.

Is this you? What are you waiting for apply now!

A day in the life of our Senior Regulatory Affairs Executive...

As  As a Senior Regulatory Affairs Executive at Wockhardt you will be a key member of the team, supporting new product development and existing licence maintenance, proposing improvements to internal systems, representing the department at internal and external meetings and providing advice on regulatory requirements.  You will prepare, submit and manage to approval new marketing authorisation applications, variations and renewals in the UK, Ireland and other markets, as required. You will also review artwork and production documentation to ensure compliance. There is an opportunity for line management for the right candidate.

What we're looking for?

You will have a degree or equivalent in life sciences, good technical knowledge of European Regulatory Affairs particularly in CMC, experience handling new marketing authorisation applications and post-licensing activities. You will be self-motivated, have an exceptional eye for detail and excellent problem-solving and decision-making capabilities. You will have the ability to multi-task and to plan and prioritise your workload to meet expected deadlines. You will be able to communicate effectively with people at all levels within and external to the organisation and to present the Company’s interests in a professional and authoritative manner.

What's in it for you?

Wockhardt offer an abundance of employee benefits and perks including; A generous pension, Death in service pay out, Generous holiday allowance, Salary sacrifice Schemes, Wockhardt Rewards website, a Sports and Social club and on-going development to name but a few.

Where will you be working?

You will be working from our Wrexham based head office which is home to our FDA and MHRA approved sterile injectable manufacturing facility. Our Wrexham site has been awarded the Investors in People Silver award for our dedication to investing in our employees, and a Bronze award from corporate health standards for promoting the health and well-being of our employees. A strong family feel, dedicated charity fundraising, fantastic potential for personal growth, and a solid benefits package make us a great place to work, so what are you waiting for apply now!

How to apply

If you are interested, please apply in writing, enclosing your CV to the Human Resources Department or alternatively, email your cv to human.resources@wockhardt.co.uk

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Sterile Technician details

Sterile Technician

Sterile Technician

 

Contract:

Permanent/Full Time

Deadline:

2nd March 2020

 

 

 Fantastic opportunities have arisen for Sterile Technicians in our cleanrooms to join our award winning Global, Pharmaceutical and Biotechnology Company you are looking to leverage your skills whilst working for one of the largest generic pharmaceutical companies in the UK? Are you self-motivated with the ability to work as part of a team? Are you a committed, flexible and enthusiastic?

(2 shifts & Nights)

Is this you? What are you waiting for apply now!

A day in the life of a Sterile Technician

You will be a key member of the team working as a Steriles Technician within the Grade B and Grade C cleanrooms at Wockhardt, ensuring that all processes are completed in accordance with cGMP. This will involve you running machinery, cleaning and processing equipment within a sterile environment. You will also process our product requirements against a programmed schedule, whilst ensuring that sterile operating procedures are followed at all times. The successful applicant would work in a specific aseptic area either operating or “servicing” high-speed automatic ampoule/vial/cartridge filling equipment.

What we're looking for;

You will be literate and numerate and be enthusiastic, as well as committed and self-motivated with a keen eye for detail and pride in your work. Experience in a regulated manufacturing environment is essential with clean room preferable. 

What's in it for you?

Wockhardt offer an abundance of employee benefits and perks including; A generous pension, death in service pay out, generous holiday allowance, salary sacrifice schemes, an online rewards hub, a sports and social club and on-going training to name but a few.

Where will you be working?

You will be working from our Wrexham based head office which is home to our FDA and MHRA approved sterile injectable manufacturing facility.Our Wrexham site has been awarded the Investors in People Silver award for our dedication to investing in our employees, and a Bronze award from corporate health standards for promoting the health and well-being of our employees. A strong family feel, dedicated charity fundraising, fantastic potential for personal growth, and a solid benefits package make us a great place to work, so what are you waiting for apply now!

How to apply

If you are interested, please apply in writing, enclosing your CV to the Human Resources Department or alternatively, email your cv to human.resources@wockhardt.co.uk

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SAP Engineering PM Coordinator details

SAP Engineering PM Coordinator

SAP Engineering PM Coordinator

 

 

Contract:

Permanent/full-time                 

Deadline:

18th February 2020

  

Do you have experience of Planned Preventative Maintenance in pharmaceutical engineering? like to solve problems with determination and focus? 

A fantastic opportunity has arisen for a SAP Engineering PM Coordinator to join our Engineering Team on a permanent contract.

Is this you? What are you waiting for apply now!

A day in the life of our Sap Engineering PM Coordinator...

To ensure that planned maintenance schedules are produced, maintained, controlled and remain compliant with business and cGMP requirements, including legislative guidelines using our SAP Planned Maintenance system.To liaise with Operations, Planning, Validation, Projects and Quality departments in order to ensure that maintenance activities are considered within the Steriles Filling, Inspection and Packaging Plans. To provide evidence that all planned maintenance tasks are scheduled, planned and completed to remain cGMP compliant at all times.

 What we're looking for?

You need to have previous experience within the Pharmaceutical Industry at management or supervisory level.With experience and competence of managing an engineering maintenance system (SAP PM is used on site), you will also be expected to attend off-site and in-house training, as appropriate, in order to maintain current awareness of technology changes likely to influence Company standards/policy and other guidelines.You will have excellent organisational and communication skills and an enthusiastic approach

What's in it for you?

Wockhardt offer an abundance of employee benefits and perks including; A generous pension, death in service benefit, generous holiday allowance, salary sacrifice schemes, Wockhardt Rewards website, a Sports and Social club and on-going professional development to name but a few.

Where will you be working?

You will be working from our Wrexham based head office which is home to our FDA and MHRA approved sterile injectable manufacturing facility. Our Wrexham site has been awarded the Investors in People Silver award for our dedication to investing in our employees, and a Silver  award from corporate health standards for promoting the health and well-being of our employees. A strong family feel, dedicated charity fundraising, fantastic potential for personal growth, and a solid benefits package make us a great place to work, so what are you waiting for apply now!

How to apply

If you are interested, please apply in writing, enclosing your CV to the Human Resources Department or alternatively, email your cv to human.resources@wockhardt.co.uk

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Quality Systems Manager details

Quality Systems Manager

Quality Systems Manager

 

 

Contract:

Permanent/full-time                 

Deadline:

19th February 2020

  

Are you are looking to leverage your skills whilst working for one of the largest generic pharmaceutical companies in the UK?

 

Do you have a quality systems experience?

 

 A fantastic opportunity has arisen for a Quality Systems Manager to join our award winning Global, Pharmaceutical and Biotechnology Company 

Is this you? What are you waiting for apply now!

Role Overview...

As the Quality Systems Manager at Wockhardt, your role will be to ensure that the site cGMP compliance is supported by Company Quality Management Systems and that the quality of products is not compromised by deficiencies in these systems.

You will drive the process of change in the site quality system towards the introduction of simpler, more flexible, more effective and more efficient mechanisms of operation, ensuring that all regulatory and company requirements for cGMP quality standards are met.

 What we're looking for?

You will have a degree (or equivalent) in a scientific discipline, with substantial experience in the pharmaceutical or medical device industries, specifically related to the management and oversight of Quality Management Systems. 

You will demonstrate effective management capability (with substantial  supervisory experience), effective written and verbal communication skills, and the ability to relate to personnel at all levels.

You will have a thorough understanding of cGMP and current best practices.

What's in it for you?

Wockhardt offer an abundance of employee benefits and perks including; A generous pension, death in service benefit, enhanced holiday allowance, salary sacrifice schemes, Wockhardt Rewards website, subsidised canteen, well-being initiatives including holistic therapies and chiropody, a Sports and Social club and on-going professional development, to name but a few.

Where will you be working?

You will be working from our Wrexham based head office which is home to our FDA and MHRA approved sterile injectable manufacturing facility. Our Wrexham site has been awarded the Investors in People Silver award for our dedication to investing in our employees, and a Silver  award from corporate health standards for promoting the health and well-being of our employees. A strong family feel, dedicated charity fundraising, fantastic potential for personal growth, and a solid benefits package make us a great place to work, so what are you waiting for apply now!

How to apply

If you are interested, please apply in writing, enclosing your CV to the Human Resources Department or alternatively, email your cv to human.resources@wockhardt.co.uk

Apply Now Cropped GIF 100 X 360

Senior Quality Systems Officer details

Senior Quality Systems Officer

Senior Quality Systems Officer

 

Contract:

Permanent/Full Time

Deadline:

25th February 2020

 

Do you have experience in site pharmaceutical quality systems? Are you an expert in cGMP, GDP or other industry best practices? Do you have an excellent eye for detail?

A fantastic opportunity has arisen for a Senior Quality Systems Officer to join our Quality Systems team on a permanent contract.

Is this you? What are you waiting for apply now!

A day in the life of a Senior Quality Systems Officer

As a Senior Quality Systems Officer at Wockhardt, you will be responsible for maintaining and improving site quality systems in line with company, corporate and international standards to support cGMP/GDP compliance and to meet business expectations.You will be responsible for leading the continuous improvement of site quality systems, such as Technical Agreements, Annual Product Reviews, Planned Change, Deviations, CAPA, Complaints and Internal Auditing through monitoring the effectiveness and level of site wide compliance, application of risk management, focussed initiatives and delivery of training, whilst maintaining associated GMP operating procedures and documentation. The role will include responsibility for the preparation of Technical Agreements and Annual Product Reviews together with any other reports and reviews necessary within the quality management system, which will require liaison with Clients and vendors to ensure all documentation is completed as defined by cGMP/GDP. You will provide support for other site projects, from a Quality Assurance perspective, by reviewing and approving where appropriate, project documentation including risk assessments, ensuring compliance with cGMP/GDP, company and other regulatory agency requirements.

What we're looking for;

You will have substantial experience within the pharmaceutical or equivalent quality assurance environment, ideally with experience of liaising with clients in relation to application and generation of technical contracts or agreements. You will have a thorough understanding of cGMP/GDP and its relationship with Technical Agreements and Annual Product Quality Reviews and other current best practices for the Pharmaceutical Quality System, and also the ability to work with concepts and practices often outside the original area of academic qualification.You will ideally have a degree (or equivalent) in a scientific discipline, membership of a recognised professional body (e.g. RSC) would be an advantage. Other key skills are a keen eye for detail, an inquisitive, analytical mindset, with effective written and verbal communication skills and the ability to use computer software systems, including SAP or equivalent and Microsoft Packages (including Excel). You will have excellent interpersonal skills with the ability to take on a supervisory role. 

What's in it for you?

Wockhardt offer an abundance of employee benefits and perks including; A generous pension, death in service benefit, enhanced holiday allowance, salary sacrifice Schemes, Wockhardt Rewards website, a Sports and Social club and on-going professional development to name but a few.

Where will you be working?

You will be working from our Wrexham based head office which is home to our FDA and MHRA approved sterile injectable manufacturing facility.Our Wrexham site has been awarded the Investors in People Silver award for our dedication to investing in our employees, and a Silver award from corporate health standards for promoting the health and well-being of our employees. A strong family feel, dedicated charity fundraising, fantastic potential for personal growth, and a solid benefits package make us a great place to work, so what are you waiting for apply now!

How to apply

If you are interested, please apply in writing, enclosing your CV to the Human Resources Department or alternatively, email your cv to human.resources@wockhardt.co.uk

Apply Now Cropped GIF 100 X 360

Engineering Technician details

Engineering Technician

Engineering Technician

 

Contract:

Permanent/Full Time

Deadline:

17th February 2020

 

Are you a Mechanically biased Engineering Technician, with experience working within the Aseptic Filling Area.

The successful candidate will provide engineering support within the Sterile Products Facility grade A, B and C areas working a shift rota basis).

Is this you? What are you waiting for apply now!

A day in the life of a Engineering Technician

Size and component changeovers on washing, filling and sealing machines for parenteral product production, Day to day maintenance on washing, filling and sealing machines for parenteral product production in compliance with cGMP. Scheduled Preventative Maintenance on washing, filling and sealing machines for parenteral product and run production in accordance with current engineering procedures and compliance with cGMP. Advise engineering supervision of machine problems, safety issues and options to improve the efficiency of machines

What we're looking for;

You must have a recognised Engineering Apprenticeship (Multi-Skilled would be an advantage), The ability to work alone or as part of a team and have excellent fault finding, rectification and communication skills. You will require an intimate understanding of pharmaceutical engineering, pharmaceutical industry standards and regulatory expectation. You will have relevant experience of working in Grade A,B and C Pharmaceutical environment and experience of working within Class 10,000 (ISO 14644-1 Class 7) and Class 100 (ISO 14644-1Class 5) environments  would be a distinct advantage.

 

What's in it for you?

Wockhardt offer an abundance of employee benefits and perks including; A generous pension, death in service benefit, enhanced holiday allowance, salary sacrifice Schemes, Wockhardt Rewards website, a Sports and Social club and on-going professional development to name but a few.

Where will you be working?

You will be working from our Wrexham based head office which is home to our FDA and MHRA approved sterile injectable manufacturing facility.Our Wrexham site has been awarded the Investors in People Silver award for our dedication to investing in our employees, and a Silver award from corporate health standards for promoting the health and well-being of our employees. A strong family feel, dedicated charity fundraising, fantastic potential for personal growth, and a solid benefits package make us a great place to work, so what are you waiting for apply now!

How to apply

If you are interested, please apply in writing, enclosing your CV to the Human Resources Department or alternatively, email your cv to human.resources@wockhardt.co.uk

Apply Now Cropped GIF 100 X 360