LSC have a great contract opportunity for a Quality Control Associate to join a Dublin based Biopharmaceutical company that specializes in secondary manufacturing activities such as Formulation, Fill Finish and Packaging.
If you have 2 years of experience working in the pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect opportunity for you!
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
- Reagent management, media preparation, GMP document review and management, sample and data management and analytical testing.
- Contributes to team by ensuring the quality of the tasks/services provided by self.
- Contributes to the completion of milestones associated with specific projects or activities within team.
- Supporting a lean culture and Right First Time (RFT).
Specific Job Duties:
- With a high degree of technical flexibility, work across diverse areas within the lab.
- Plan and perform routine tasks with efficiency and accuracy.
- Review, evaluate, back-up/archive, and approve analytical data.
- Troubleshoot, solve problems and communicate with stakeholders.
- Participate in audits, initiatives, and projects that may be departmental or organizational in scope.
- Evaluate lab practices for compliance and operational excellence improvement on a continuous basis.
- Participate in lab investigations and approve lab results.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- Demonstrated ability to work independently and deliver right first time results.
- Works under minimal direction.
- Work is guided by objectives of the department or assignment.
- Follows procedures.
- Refers to technical standards, principles, theories and precedents as needed.
- May set project timeframes and priorities based on project objectives and ongoing assignments.
- Demonstrated leadership and communication skills.
- Auditing documentation and operation process.
- Demonstrated ability to interact with regulatory agencies.
Relevant Experience:
* Bachelor's degree in a science discipline.
* 1-2 years of biopharmaceutical QC experience or related quality control or GMP laboratory experience in the pharmaceutical or medical device industry.
* Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products.
Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a Stamp 1G/Stamp 4 visa to apply!
Apply via this advert or contact Jenny Murphy on 021 4777329 if you have anymore questions about this role!
