PQA Trainer
- Denmark
- Contract
- Compliance / Quality Assurance
Our client, a global CDMO in pharmaceutical manufacturing, is recruiting for a PQA Trainer to join their new and exciting large-scale CAPEX investment programme. With a mission to provide process development and cGMP production in cell culture, microbial fermentation, and gene therapies, this is an outstanding opportunity make a genuine contribution to the bio-pharmaceutical industry.
Responsibilities include:
- Maintain a systematic and continuous focus on ensuring the appropriate curricula are assigned to employees they are dedicated to support (PQA or entire project).
- Plan and prioritise which curricula new employees must have assigned together with other work-stream training partners.
- Ensure employees have required and relevant curricula assigned
- Standardise required training for tasks within the team.
- Align training requirements with other teams.
- Serve as first point of contact on learning matters within team(s) they support.
- Defining the training strategy for the Expansion projects.
- Ensure OJT and ILC trainers are available.
- Support development of training material for both eLearning, ILC and OJT training.
- Support development of training curricula and creation of classes.
- Training partner for PQA wrt, (incl. non GMP training)
- Input to the Quality Risk Register.
- Requires extensive experience including experience with design and construction projects for pharmaceutical manufacturing facilities.
- Solid technical background and experience in Bio and pharmaceutical production.
- Solid QA Experience is a requirement.
- Solid technical background and experience.
- Ability to keep work pace and meet deadlines. Good organising and planning skills.
- Demonstrated proficiency communicating and collaborating at a variety of levels.
- Strong communication skills. Problem solver with a focus on achievement of overall project goals.
- Computer skills (Compliance-wire & EIDA)
If this role is of interest, please apply now!
#LI-ML1
We have worked together with QCS Staffing for seven years now and have always received a professional service. QCS Staffing's speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of QCS Staffing's people and their ability to deliver.
Global Pharmaceutical firm
I have always received a highly professional & personable service from the team at QCS Staffing. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
Save as job alert
Similar Jobs
Salary
Competitive
Location
Kalundborg
Salary
Competitive
Sector
Compliance / Quality Assurance
Job type
Contract
Location
Denmark
Description
Planner - Denmark , Kalundborg - 12 Month Contract Our client, a global pharmaceutical company, are looking for a Planner to join their team. The company has grown to become a world leader in the
Reference
36928
Expiry Date
01/01/0001
Author
Alex StanfordAuthor
Alex StanfordSalary
Competitive
Location
Texas
Salary
Competitive
Sector
Compliance / Quality Assurance
Job type
Contract
Location
North America
United States
Description
Construction Manager - Texas - 6 Month Contract How would you like the opportunity to work with in one of the largest biopharmaceutical projects in the country? If yes, then this is the
Reference
36986
Expiry Date
01/01/0001
Author
Narda RiveraAuthor
Narda RiveraSalary
Competitive
Location
North Carolina
Salary
Competitive
Sector
Compliance / Quality Assurance
Job type
Contract
Location
North America
East Coast
Description
Document Review Specialist - US, North Carolina - 6-12 Month Contract Our client, a global pharmaceutical manufacturing organization are looking for a talented Document Review Specialist to join
Reference
37009
Expiry Date
01/01/0001
Author
Mark ChaumetonAuthor
Mark ChaumetonInsights
Send us your CV
Our candidates are the cornerstone of our organisation and we are always looking to connect with new professionals who are seeking their next contract assignment or career opportunity.
Megan
I manage this role.