Job Description
An amazing opportunity has arisen for a QC Laboratory Manager. You will provide laboratory support, expertise and co-ordination of analysis, release and testing of samples to support Quality release of product. You will contribute to the High-Performance culture within the Quality CoE by providing an inclusive environment to enable team members to achieve their best work.
What you will do:
Bring energy, knowledge, innovation and leadership to carry out the following:
Supervision and co-ordination of a 4 shift team within Quality laboratories to ensure the timely and efficient testing and reporting of QC samples.
* Co-ordination of area resources.
* Ensure testing is completed within required time frames
* Supervision of area personnel.
* Training of area personnel.
* Participate in corporate/regulatory audits.
* Delivery of area performance to meet or exceed performance or quality goals.
* Contribute to site management operational and strategic initiatives.
* Liaising with external vendors.
* Ensure compliance with cGMP and other business compliance regulations.
* Lead, promote, participate and supervise the implementation and maintenance of the SHE programmes relevant to you.
* Participate in risk assessments, inspections, audits, incident investigations, etc. and implement and follow-up CAPA’s assigned to you.
* Accountable for driving a culture of Continuous Improvement by deploying Six Sigma tools.
What skills you will need:
In order to excel in this role, you will more than likely have:
* At least 5 years’ experience in the Pharmaceutical industry or a similar operating environment which includes experience in a QC Laboratory or equivalent – as applicable
* 3rd level Degree in Science or related discipline
* Knowledge of working practices required for a QC laboratory
* Good verbal and written communication skills
* Ability to plan and organize effective and efficient work schedules
* Demonstrated ability to problem solve and action changing priorities
* Demonstrated ability to fully realize improvement initiatives
As a company, we are committed to ‘Inventing for Life’ in all that we do. We keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of the world’s most challenging healthcare needs.
We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment.
So, if you are ready to:
Invent solutions to meet unmet healthcare needs, Impact the future by driving one of the world’s leading healthcare companies, and inspire your team to reach their full potential and push the boundaries of science and technology, please apply today.
Current Employees apply HERE
Current Contingent Workers apply HERE
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
Regular
Relocation:
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
Not Applicable
Shift:
Valid Driving License:
Hazardous Material(s):
Required Skills:
Accountability, Accountability, Analytical Method Transfer, Analytical Testing, Analytical Thinking, cGMP Compliance, Corrective Action Management, Driving Continuous Improvement, GMP Documentation, Incident Investigations, Inclusive Leadership, Innovation, Instrumentation, Laboratory Operations, Management Process, People Leadership, Pharmaceutical Management, Pharmaceutical Quality Control (QC), Program Implementation, Project Implementations, Quality Standards, Regulatory Compliance, Risk Assessments, Site Management, Six Sigma {+ 4 more}
Preferred Skills:
Job Posting End Date:
08/23/2025
*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Requisition ID:R361473
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