Wockhardt's Current Vacancies

Main Recruitment Page

Regulatory Affairs Officer details

Regulatory Affairs Officer

Regulatory Affairs Officer

Contract:

Permanent/full-time]

Deadline:

20th January 2020

 

Are you a recent graduate in life sciences looking for your first step into industry or a pharmaceutical professional looking to move into Regulatory Affairs? Are you a quick learner who enjoys working in a fast-paced environment and handling multiple projects?

Then look no further, a fantastic opportunity has arisen for a Regulatory Affairs Officer to join the Regulatory Affairs team 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 Regulatory Affairs Officer...

As one of the Regulatory Affairs Officers at Wockhardt, you will be a key member of the team, preparing and submitting post-licence maintenance applications, including quality and safety variations, labelling changes and renewals. You will also have specific responsibility for administering the electronic regulatory management system.This role provides a great opportunity to gain a broad experience in all aspects of Regulatory Affairs. With over 600 marketing authorisations worldwide and a strong new product pipeline, this is a challenging and fast-paced environment to work in.

What we're looking for?

You will be a quick learner with good organisation skills and the ability to work under your own initiative. You will have an exceptional eye for detail, strong verbal and written communication skills and a high degree of comfort working with electronic systems. You will be able to work under pressure whilst managing multiple projects and meeting tight deadlines. You will have a degree in life sciences, pharmacy or a pharmaceutical-related subject. Experience in the pharmaceutical industry is advantageous but not required.

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

Apply Now Cropped GIF 100 X 360

Senior Regulatory Affairs Executive details

Senior Regulatory Affairs Executive

Senior Regulatory Affairs Executive

Contract:

Permanent/full-time]

Deadline:

20th January 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

Apply Now Cropped GIF 100 X 360

Sterile Technician details

Sterile Technician

Sterile Technician

 

Contract:

Permanent/Full Time

Deadline:

3rd Decemeber 2019

 

 

 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

Apply Now Cropped GIF 100 X 360

SAP Engineering PM Coordinator details

SAP Engineering PM Coordinator

SAP Engineering PM Coordinator

 

 

Contract:

Permanent/full-time                 

Deadline:

29th January 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 Supply Quality Officer...

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

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

Quality Systems Officer details

Quality Systems Officer

Quality Systems Officer

 

Contract:

Permanent/Full Time

Deadline:

13th January 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 broad knowledge of Pharmaceutical Quality Systems and the ability to multi-task within tight timelines? Do you have excellent interpersonal skills and meticulous attention to detail?

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

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

A day in the life of a Quality Systems Officer

As a Quality Systems Officer here at Wockhardt you will mainly focus on the preparation of Annual Product Quality Reviews, including analysis and interpretation of the associated data, co-ordination and investigation of Quality Complaints, as well as preparation of Technical Agreements. This will require an ability to apply acquired technical knowledge and liaise with Clients and customers to achieve satisfactory completion of the required objectives. Other role duties will include maintaining the site quality system in a manner that is GMP compliant and meets business expectations and timescales. This will include timely execution of deviation investigations, Planned Change actions as well as Corrective and Preventive actions. The Quality Systems Officer will also share the responsibility for monitoring the effectiveness and level of site wide compliance of all quality systems and quality targets. 

What we're looking for;

Ideally a graduate (or equivalent) in a scientific discipline. Membership of a recognised professional body (eg RSC) would be advantage but is not essential. Previous experience within the pharmaceutical industry or equivalent quality assurance/control environment. A thorough understanding of cGMP, GAMP and other current practices would be an advantage and Excellent written, verbal communication and interpersonal skills is 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, 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