Quality Control Analyst
  Negotiable
  Queenborough, Kent
  permanent,full-time

This Job Has Expired! This advert has now been deleted by the advertiser, the details below are for information only.


This role will be part of our quality control team who test both raw materials and finished products to ensure they conform to the standards required.

Some of the duties will include;

• Testing and analysing pharmaceutical drugs to determine their identity, purity and strength according to GMP principles.
• Collect and record receipt of samples from various sources and prepare for analysis.
• Undertake the analysis of incoming samples and finished products to documented specifications using conventional analytical techniques e.g. HPLC and GC
• Ensure that pharmaceutical products are stored properly.
• Liaise with other professionals regarding the development, manufacturing and testing of pharmaceutical products.
• Prepare analytical reagents/media/cultures for general laboratory use.
• Ensure that any waste materials are processed, recorded and disposed in accordance with cGLP, safety and environmental requirements.
• Ensure all activities are performed in compliance with customer and ICH procedures.
• Ensure that all instruments are calibrated and adequately maintained prior to use.
• Verify laboratory data and ensure accurate primary records are kept, report any anomalies or out of specification results to Section Leader.
• Maintain and support the Stability program with respect to: Stability Diary, Stability Reports, Stability sampling programme, New product introductions and PCN requirements
• Review stability indicating methods.
• Generate stability reports suitable for inclusion in regulatory dossiers.
• Actively contributes to Laboratory Improvement activities.

About you

We are looking for somebody that has some experience of analytical techniques such as HPLC and GC. A HND or Degree in chemistry would be an advantage.

What we offer

Above all, you can expect a safe, modern, friendly and collaborative working environment. We regularly benchmark ourselves against our industry and we are confident that we offer a competitive salary and benefits packages to all our colleagues.

• Competitive base salary
• 27 days plus statutory holidays
• A defined contribution company pension scheme
• Life assurance (equivalent to four times your salary)
• Cycle-to-work scheme
• Childcare vouchers
• All-employee share incentive scheme

We want to provide an environment where our colleagues play an active part in the growth of our business. A challenging but supportive environment where talented people can really grow and take advantage of a wide range of diverse opportunities that we offer.

About Aesica

We are a leading pharmaceutical CDMO that delivers the high-quality active pharmaceutical ingredient (API) and finished dose formulation development and manufacturing services the industry demands.

Our state-of-the-art facilities are home to around 1,300 colleagues across six development, manufacturing and operational sites in the UK, Germany and Italy. We are particularly proud of the diverse workforce that we have built. It is this healthy mix of experienced pharmaceutical professionals and ambitious talent that helps us deliver on our business promises of expertise and innovation.

Apply

If this sounds like the ideal role for you then we’d love to hear from you. Please click the “apply online” button and follow the prompts.


Advertiser: Direct Employer

Reference:

Posted on: 2018-09-18 09:26:31

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This Job Has Expired! This advert has now been deleted by the advertiser, the details below are for information only.


This role will be part of our quality control team who test both raw materials and finished products to ensure they conform to the standards required.

Some of the duties will include;

• Testing and analysing pharmaceutical drugs to determine their identity, purity and strength according to GMP principles.
• Collect and record receipt of samples from various sources and prepare for analysis.
• Undertake the analysis of incoming samples and finished products to documented specifications using conventional analytical techniques e.g. HPLC and GC
• Ensure that pharmaceutical products are stored properly.
• Liaise with other professionals regarding the development, manufacturing and testing of pharmaceutical products.
• Prepare analytical reagents/media/cultures for general laboratory use.
• Ensure that any waste materials are processed, recorded and disposed in accordance with cGLP, safety and environmental requirements.
• Ensure all activities are performed in compliance with customer and ICH procedures.
• Ensure that all instruments are calibrated and adequately maintained prior to use.
• Verify laboratory data and ensure accurate primary records are kept, report any anomalies or out of specification results to Section Leader.
• Maintain and support the Stability program with respect to: Stability Diary, Stability Reports, Stability sampling programme, New product introductions and PCN requirements
• Review stability indicating methods.
• Generate stability reports suitable for inclusion in regulatory dossiers.
• Actively contributes to Laboratory Improvement activities.

About you

We are looking for somebody that has some experience of analytical techniques such as HPLC and GC. A HND or Degree in chemistry would be an advantage.

What we offer

Above all, you can expect a safe, modern, friendly and collaborative working environment. We regularly benchmark ourselves against our industry and we are confident that we offer a competitive salary and benefits packages to all our colleagues.

• Competitive base salary
• 27 days plus statutory holidays
• A defined contribution company pension scheme
• Life assurance (equivalent to four times your salary)
• Cycle-to-work scheme
• Childcare vouchers
• All-employee share incentive scheme

We want to provide an environment where our colleagues play an active part in the growth of our business. A challenging but supportive environment where talented people can really grow and take advantage of a wide range of diverse opportunities that we offer.

About Aesica

We are a leading pharmaceutical CDMO that delivers the high-quality active pharmaceutical ingredient (API) and finished dose formulation development and manufacturing services the industry demands.

Our state-of-the-art facilities are home to around 1,300 colleagues across six development, manufacturing and operational sites in the UK, Germany and Italy. We are particularly proud of the diverse workforce that we have built. It is this healthy mix of experienced pharmaceutical professionals and ambitious talent that helps us deliver on our business promises of expertise and innovation.

Apply

If this sounds like the ideal role for you then we’d love to hear from you. Please click the “apply online” button and follow the prompts.


Advertiser: Direct Employer

Reference:

Posted on: 2018-09-18 09:26:31

I want to receive the latest job alerts for:

jobs in Queenborough, Kent

By creating a job alert, you agree to our Terms . You can change your consent settings at any time by unsubscribing or as detailed in our terms.

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  New Appointments Group

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