Wockhardt's Current Vacancies

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Engineering Technician details

Engineering Technician

Engineering Technician

 

 

Contract Type

12 month contract              

Deadline:

21st April 2021

  

4 on 4 off Shifts, Days & Nights, rotating

7 am to 7 pm Days and 7 pm to 7 am Nights

A fantastic opportunity has arisen for Engineering Technicians to support our Inspection & Packing Team on a 12 month contract.

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

Role Overview...

You will be the engineering expert for automatic vision inspection, labelling and deep-draw blister packaging for pharmaceutical containers, which will be predominantly 5  millilitre vials. Duties will include end of day and end of batch strip downs of equipment to facilitate cleaning, rebuilds after cleaning and adjustments to ensure that inspection and packaging activities run smoothly and meet the output requirements of the busy manufacturing environment.

You will be able to work on your own or as part of the Packing & Inspection team in accordance with Good Manufacturing Practice. This is a position for a dynamic, motivated and enthusiastic engineer from any discipline, but with strong mechanical knowledge. Electro-mechanical experience is desirable but not essential. Training will be delivered by current Packing & Inspection Engineers under the current training programme.

 What we're looking for?

Experienced in providing engineering support in a Sterile Inspection & Packing Department, you will hold a recognised Engineering Apprenticeship/HND/HNC/degree in an engineering discipline.

You will be competent in working alone or as part of a team and have excellent diagnostic, rectification and communication skills.

A thorough understanding of pharmaceutical engineering and regulatory requirements in essential.

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 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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Senior Regulatory Affairs Executive details

Senior Regulatory Affairs Executive

Senior Regulatory Affairs Executive

 

 

Contract:

Permanent/Full Time                 

Deadline:

15th April 2021

  

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!

 

Role Overview...

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.

 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 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 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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QA Inspector details

QA Inspector

QA Inspector

 

 

12 month Contract/full-time                 

Deadline:

26th April 2021

 

Monday to Friday, 8:15am – 4:15pm

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

Look no further! A fantastic opportunity has arisen for a QA Inspector to join our award winning Global, Pharmaceutical and Biotechnology Company on a 12 month contract.

Role Overview...

The successful candidate will be required to work as part of the Quality Assurance team, to assist with ensuring the continued compliance of the Wrexham site with both Company and International Quality Standards. This will include a combination of technical, administrative, and documentation review responsibilities and tasks.

What we are looking for?

Ideally applicants will possess two A levels (or equivalent), however 5 GCSE’s (or equivalent) including Maths and English is required as a minimum. Previous experience of processing documentation and a working knowledge of GMP would be an advantage, but is not essential, as on-going training will be provided via a recognised structure. Candidates will be expected to possess good self-motivational skills, giving meticulous attention to detail, and showing the ability to work with reduced supervision. In addition the candidate should be able to demonstrate good communication skills and have good computer 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, well-being initiatives including holistic therapies and chiropody, a Sports and Social club, onsite canteen and on-going professional development, to name but a few.

Where will you be working?

You need to be computer literate and self-motivated.   You must possess a minimum of 4 GCSE qualifications (or equivalent).  Previous experience of working in a laboratory or warehouse environment with a working knowledge of cGMP and SAP would be an advantage but is not essential, as training will be provided via a recognised structure.  

How to apply

If you are interested, please apply in writing, enclosing your CV to hello@marketplacetechnical.co.uk

 

Senior Formulation Scientist details

Senior Formulation Scientist

Senior Formulation Scientist

 

Contract:

Permanent/full time                 

Deadline:


Date: 16th April 2021  

Are you practical, with an analytical mind? Do you like to solve problems with determination and focus?  Highly motivated with a drive to succeed?

A fantastic opportunity has arisen for a Senior Formulation Scientist to join our Research and Development team on a permanent contract!

Role Overview...

As a Senior Formulation Scientist at Wockhardt, you will be a key member of the team and your main responsibilities will be developing new products and undertaking formulation development studies to support regulatory filings and production. Responsible for the design and implement formulation development studies, whilst maintaining good written records of experimental results, given both verbal and written reports of progress. Accurate analysis and calculation of results, in line with written protocol and /or SOPs of the company, and participate in practical problem solving in relation with on-going and new projects, whilst maintaining effective communication with relevant departments and external  service providers.

 What we're looking for?

A Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences or related scientific discipline is desirable, with strong verbal and written communication skills with the ability to work effectively with team members and internal / external customers.Significant experience of products development, preferably in the pharmaceutical industry in generic parenteral and oral liquid drug products, with exceptional eye for detail and excellent problem-solving and decision-making capabilities is required. Must have a thorough knowledge of formulation development, process development and scale up and in-depth knowledge of the product development cycle and ability to establish a product development plan.,Experience with technology transfers both internally and externally and good organisational skills, ability to respond to multiple priorities simultaneously and familiar with CMC Regulatory documents to support MAA would also be advantage.  

What's in it for you?

You will have a positive, proactive and enthusiastic approach, enjoy working as part of a busy team, as well as strong organisational, administrative and communication skills.  You will have experience of using MS Project, Excel and MS Office packages.Educated to degree level (or equivalent), it is essential that you are experienced in coordinating and keeping up to date project management plans and proactively driving tasks to completion to agreed timescales. Pharmaceutical industry experience is highly desirable.

Where will you be working?

You will be working from our Wrexham based head office which is home to our 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 details

Senior Supply Quality Officer

Senior Supply Quality Officer

 

 

Contract:

Permanent/Full Time                 

Deadline:


Date  28th April 2021

Are you are looking to leverage your skills whilst working for one of the largest generic pharmaceutical companies in the UK? Are you a strategic thinker with a broad knowledge of Pharmaceutical Quality Assurance? Do you have Excellent Interpersonal skills and meticulous attention to detail?

Look no further! A fantastic opportunity has arisen for a Senior Supply Quality Officer to join our award winning Global, Pharmaceutical and Biotechnology Company

Role Overview...

As a Senior Supply Quality Officer here at Wockhardt you will be responsible for managing a number of third party suppliers of finished products (sterile and non-sterile formulations) and raw materials in relation to cGMP standards. You will also be a key point of contact for new projects covering new product introduction and existing product site transfers. Your role is 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 perform GMP audits of third party manufacturers to Wockhardt and provide technically competent contact for third party technical issues with regard to product quality issues and business improvement.

 What we're looking for?

Ideally applicants will possess a relevant degree level qualification or equivalent in chemistry/pharmacy/biology as well as Quality Assurance experience in relation to sterile injectable products. Candidates will have previous experience in a quality driven environment, risk analysis experience and have good knowledge of EU GMP. You will have the ability to perform root cause analysis with a proven ability to manage multiple projects and tasks. Effective written and verbal communication skills are essential along with the ability to work effectively in a cross-functional team. Candidates will be results driven and possess a can-do attitude.

What's in it for you?

You will have a positive, proactive and enthusiastic approach, enjoy working as part of a busy team, as well as strong organisational, administrative and communication skills.  You will have experience of using MS Project, Excel and MS Office packages.Educated to degree level (or equivalent), it is essential that you are experienced in coordinating and keeping up to date project management plans and proactively driving tasks to completion to agreed timescales. Pharmaceutical industry experience is highly desirable.

Where will you be working?

You will be working from our Wrexham based head office which is home to our 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