Wockhardt's Current Vacancies

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Assistant Manager Warehouse Operations details

Assistant Manager Warehouse Operations

Assistant Manager Warehouse Operations

 

Contract:

Permanent/Full Time

Deadline:

25th October 2019

 

Are you are looking to Leverage your skills whilst working for one of the largest generic pharmaceutical companies in the UK? Are you Quality Driven with a keen eye for detail? Do you have previous experience in both FMCG Warehouse/Goods inward function and a supervisory role and a good understanding of GDP?

 Look no further! A fantastic opportunity has arisen for an Assistant Manager within Distribution to join our award winning Global, Pharmaceutical and Biotechnology Company.

A day in the life of our Assistant Manager 

To ensure on a daily basis the timely and accurate servicing of customers (internal and external) to meet the business requirements whilst adhering to GMP, budgetary, Home Office and Health and Safety requirements, whilst managing the daily activities and oversee the accurate and speedy processing of all items coming into and leaving the Warehouse, whilst working to tight deadlines and adjusting to meet the changing needs required.To provide supervisory support and ensure the training is developed to all Warehouse Team Leaders and Warehouse Operatives.

What we're looking for;

You should have a good basic educational standard with excellent IT skills. High calibre interpersonal, communication and motivational skills are essential. Have the ability to work on your own initiative.A thorough understanding of current GMP, Health and Safety and COSHH regulation and must have a clear and valid CRB certificate. 

 

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

QA Officer details

QA Officer

QA Officer

 

Contract:

Permanent/Full Time

Deadline:

11th November 2019

 

Are you are looking to leverage your skills whilst working for one of the largest generic pharmaceutical companies in the UK? Are you highly motivated with substantial experience within the Pharmaceutical industry? Do you have strong quality compliance background and possess problem solving abilities?

Look no further! A fantastic opportunity has arisen for a QA Officer to join our award winning Global, Pharmaceutical and Biotechnology Company on a permanent contract, working a 6am-2pm / 1.30pm-9.30pm shift system!

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

A day in the life of a QA Officer

As a QA Officer working at Wockhardt you will focus on mainly on the routine review of batch and other GMP documents to support QA batch review and QP release, and improving processes to drive down non-conformances and failures. The duties will include effective reporting and investigation of incidents and deviations and other batch related and non-batch related investigations, and working in multifunctional teams to identify and drive process improvements. Other routine tasks are defined within the Job Description, which is available on request.

What we're looking for;

You should have a degree or equivalent in Chemistry, Pharmacy or other appropriate life sciences, effective written and verbal skills, quality audit experience would also be preferable. We would also like you to have substantial experience within a pharmaceutical industry preferably within Quality Assurance, Production or Quality control. 

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

Quality Assurance Specialist details

Quality Assurance Specialist

Quality Assurance Specialist

 

Contract:

Permanent/Full Time

Deadline:

27th November 2019

 

   Do you have experience in sterile product manufacture? Do you have substantial experience in the quality functions with in pharmaceutical industry?

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

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

A day in the life of a Quality Assurance Specialist

As a Quality Assurance 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 work closely with production and engineering teams to ensure that current industry standards are applied to the manufacture of sterile pharmaceutical products, taking a lead within the QA department to plan and organise work to agreed deadlines, including management and support for manufacturing/engineering teams in relation to non-conformances and non-conforming product, to meet the requirements of cGMP and equivalent standards as appropriate.

What we're looking for;

You will be experienced in the current industry standards for finished product release, which practical experience in risk management, internal audit, non-conformances, deviations and CAPA.  You will have experience in the use of risk assessment procedures as described in Industry guidelines such as ICH Q9 in order to determine the requirements of processes required to achieve a satisfactory product.  You will have the drive and desire to make positive change and the ability to lead teams to deliver improvements, in compliance with all relevant regulations to reduce risk and to ensure patient safety and product efficacy.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.Experience of process improvement techniques would be an advantage.

What's in it for you?

You will be literate and numerate, demonstrating enthusiasm, as well as being committed and self-motivated with a keen eye for detail and pride in your work. You will have experience in a Warehouse environment previously, and ideally be competent in fork lift truck duties. Knowledge of administration and computer systems is essential for this role although training will be given. A previous experience of working in a GDP environment and an interest in workplace health & safety would be an advantage

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:

3rd December 2019

 

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