laboratory analyst Work, Jobs in swindon, wil (with Salaries)

QC Analyst II
Thermo Fisher Scientific —Swindon
- Weekend availability
2d
Laboratory Analyst
Ecolab Inc. —Andover
- Full-time
- Engineering
- Laboratory experience
- Microsoft Office
- Employee stock purchase plan
3d
Laboratory Analyst I
Abbott Laboratories —Witney
- Full-time
- Laboratory experience
- Bachelor's degree
- Communication skills

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QC Analyst II
Thermo Fisher Scientific —Swindon
To perform quality control analytical testing of incoming goods, intermediates and/or finished products under cGMP conditions for QC release or as part of…
2d
Laboratory Analyst
Ecolab Inc. —Andover
The opportunity to take on some of the world’s most meaningful challenges, helping customers achieve clean water, safe food, and healthy environments.
3d

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QC Analyst II

Thermo Fisher Scientific -
Swindon

Apply Now

Job details

Full-time
2 days ago

Full job description

Work Schedule

Rotational days/weekends

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cold Room/Freezers -22degreesF/-6degrees C, Laboratory Setting, Loud Noises (Equipment/Machinery), Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biological products etc.), Will work with hazardous/toxic materials

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

DESCRIPTION:

This role is responsible for the performing routine laboratory procedures, transfer/verification/validation of methodology, and project work within the department to support manufacture and release of pharmaceutical products.

Responsibilities:

To perform quality control analytical testing of incoming goods, intermediates and/or finished products under cGMP conditions for QC release or as part of stability studies.

To prepare technical documentation including but not limited to analytical write-ups, standard operating procedures, specifications, investigations and reports.

To perform planned preventative maintenance and performance calibrations on equipment.

To perform transfer/verification/validation of laboratory procedures within the team where required.

To assist with technical troubleshooting related to analytical equipment, analytical methods or unexpected results

To maintain own training records and support and train other team members as required.

To participate in continuous improvement activities and look for further opportunities to progress the team/department.

To communicate effectively with others on site and internationally, and to participate with them in problem solving activities.

Ensure cGMP is applied in their area of work and comply with cGMP in all areas of the business.

To work with HSE, cGMP and 5S in mind at all times.

To carry out any other tasks which may be required from time to time.

EH&S:

Understand emergency procedures and comply with safe systems of work.

Ensure compliance with environment, health and safety and security policies and procedures, rules, signage and instructions at all times

Ensure prompt reporting and investigation of all accidents, near misses and breaches of rules

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