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Supply Quality Specialist details

Supply Quality Specialist

Supply Quality Specialist

 

Contract:

Permanent/Full Time

Deadline:

24th May 2019 

 

Do you have experience in technology/product transfer? Do you have substantial experience in the quality functions with in pharmaceutical industry?

A fantastic opportunity has arisen for a Supply Quality Specialist to join our Supply Quality team on a permanent contract.

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

A day in the life of a Supply Quality Specialist

As the Supply Quality Specialist at Wockhardt, your role will be to ensure that products are manufactured and processed in accordance with company, corporate and international standards with respect to cGMP, product safety, quality and efficacy.You will ensure that current industry standards are applied to the transfer of CP Pharmaceutical/Wockhardt UK MA’s such as described in the ISPE Good Practice Guides for technology transfer and operations management.You will also be required to ensure that the requirements of GAMP and equivalent standards are applied as appropriate with third party suppliers. 

What we're looking for;

You will be experienced in the current industry standards for technology/product transfer as given in current regulations and guides such as the ISPE good practice guides. You will have experience in the extensive use of risk assessment procedures as described in Industry guidelines such as ICH Q9 in order to determine the type and extent of process required to achieve a satisfactory product / technology transfer and subsequent management of the contract manufacturing site being used. You will have the ability to work with concepts and practices outside the original area of academic qualification and apply them effectively in terms of GMP/QA matters.You will have a degree (or equivalent) in a scientific discipline, with substantial experience in the pharmaceutical industry, preferably with experience within a quality function, including some auditing experience. Other key skills are a keen eye for detail and effective written and verbal communication skills. 

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

Senior Supply Quality Officer - Supply Specialist details

Senior Supply Quality Officer - Supply Specialist

Senior Supply Quality Officer - Supply Specialist

 

Contract:

Permanent/Full Time

Deadline:

24th May 2019 

 

Do you have experience in the quality functions with in pharmaceutical industry? Have you got auditing experience?

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

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

Role Overview

As the Senior Supply Quality Officer – Supply Specialist at Wockhardt, your role will be to ensure that products manufactured for Wockhardt UK are manufactured and processed in accordance with company, corporate and international standards with respect to cGMP, product safety, quality and efficacy.You will be required to assist in implementing current industry standards are applied to the transfer of CP Pharmaceutical/Wockhardt UK MA’s such as described in the ISPE Good Practice Guides for technology transfer and operations management. Experience in the use of industry standard risk assessment process such as ICH Q9 would be an advantage.You will also be to assist in ensuring that the requirements of GAMP and equivalent standards are applied as appropriate with third party suppliers. 

 

What we're looking for;

You will have substantial experience in the pharmaceutical industry, preferably with experience within a quality function, including some auditing experience. You will have the ability to work with concepts and practices outside the original area of academic qualification and apply them effectively in terms of GMP/QA matters.You will have a degree (or equivalent) in a scientific discipline. Other key skills are a keen eye for detail and effective written and verbal communication skills.

 

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

Apply Now Cropped GIF 100 X 360

Security Officer details

Security Officer

Security Officer

 

Contract:

Permanent/Full Time

Deadline:

23rd July 2019 

 

Are 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?

Do you have experience of providing a professional and approachable service to a busy Security function?

Look no further! A fantastic opportunity has arisen for a Security Officer to join our Security Team, working 12 hour shifts on a 4 on 4 off basis.

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

A day in the life of a Security Officer

Reporting to the Security Manager, the successful candidate will work as part of our in-house Security team providing the site with an effective and efficient security service to internal and external customers in line with established customer service practices and procedures.

What we're looking for;

You must have relevant Security experience and be able to demonstrate excellent communication skills both verbal and written,   be computer literate, with a sound knowledge of word. Attainment of the SIA and First Aid are essential.  

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

Apply Now Cropped GIF 100 X 360

Senior Quality Systems Officers details

Senior Quality Systems Officers

Senior Quality Systems Officers

Contract:

Permanent/full-time]

Deadline:

31st April 2019

 

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

A fantastic opportunity has arisen for two Senior Quality Systems Officers to join our Quality Systems team on permanent contracts.

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

 

A day in the life of our Senior Quality Systems Officers......

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 compliance and to meet business expectations.You will be responsible for leading the continuous improvement of site quality systems, such as Planned Change, Deviations, Complaints and Self-Inspection 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 also support 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. You will provide support for other site projects, from a Quality Assurance perspective, including the validation of automated systems, by reviewing and approving where appropriate, project documentation including risk assessments, ensuring compliance with cGMP, company and other regulatory agency requirements.

What are we looking for:

You will have substantial experience within the pharmaceutical or equivalent quality assurance/control environment. You will have a thorough understanding of cGMP, GAMP and other current best practices, and also the ability to work with concepts and practices often outside the original area of academic qualification.You will 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 Excel. The ability to use statistical techniques to analyse data would also be an advantage. 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

Responsible Person (RP) details

Responsible Person (RP)

Responsible Person (RP)

 

Contract:

Permanent/Full Time

Deadline:

23rd July 2019 

 

Are you an MHRA recognised Responsible Person with experience in overseeing EU distribution and Export operations?

A fantastic opportunity has arisen for a Responsible Person to join our QA team on a permanent contract.

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

Role Overview

As the Responsible Person at Wockhardt, you will be responsible for ensuring that the distribution activities are in compliance with the GMP/GDP requirements. The role will work closely with the business operations departments to ensure that the quality requirements will be met for all export and out-licencing arrangements.

You will also ensure that the distribution activities conducted by Wockhardt UK are performed in accordance with the applicable regulations and serve as the Responsible person on Wockhardt UK WDL.

What we're looking for;

You will be currently recognised by the MHRA as a Responsible Person. You will have previous experience overseeing Export operations under WDA(H). It is not essential, but desirable that you will be a graduate (or equivalent) in a scientific discipline.

Previous experience at a commercial drug product manufacturing site in a quality function is desirable. Professional written and verbal communication skills and the ability to foster excellent working relationships with peers and management are essential.

You will have an analytical mind, good problem solving skills and the ability to multi-task. You will have the ability to work in the spirit of continuous improvement and innovation, and creatively open to new ideas and methods.

 

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

Apply Now Cropped GIF 100 X 360

Quality Compliance Manager (QP) details

Quality Compliance Manager (QP)

Quality Compliance Manager (QP)

 

Contract:

Permanent/Full Time

Deadline:

23rd July 2019 

 

Are you an MHRA recognised qualified person with experience of aseptic sterile manufacturing batch release? Do you have substantial experience within the pharmaceutical industry?

A fantastic opportunity has arisen for a Quality Compliance Manager (QP) to join our QA team on a permanent contract.

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

Role Overview

As the Quality Compliance Manager (QP) at Wockhardt, you will be responsible for certifying batches of medicinal products prior to release for sale and placing on the market. You will have the full responsibility of undertaking the duties of a qualified person in accordance with the professional code of practice.You will also be required to audit the quality systems and procedures in use within Wockhardt UK against compliance to cGMP and to make recommendations for quality improvement corrective actions.This role will also involve the direct line management of a group of Quality Assurance Officers.

What we're looking for;

You will be an MHRA recognised Qualified Person under directives 2001/EC, 2001/83/EC and 2001/20/EC. You will be a graduate (or equivalent) in Chemistry, Pharmacy, or other appropriate discipline with substantial experience within the pharmaceutical industry, specifically within QA, including management of teams. Quality auditing experience is also essential.

You will have the ability to work with concepts and practices outside the original area of academic qualifications and to apply them effectively in terms of GMP/QA matters.

Effective written and verbal communication skills and the ability to relate to all levels are essential.

As a QP, you must be able to demonstrate that you maintain up-to-date knowledge and experience in both technical and scientific progress and of changes in quality management relevant to the products being released.

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

Apply Now Cropped GIF 100 X 360