About the Company
Merck & Co., Inc. is a global healthcare leader working to help the world be well. From developing new therapies that treat disease to helping people in need, we are committed to improving health and well-being around the world. Our mission is to discover, develop, and provide innovative products and services that save and improve lives.
Job Description
We are seeking a highly motivated and skilled QC Chemist to join our quality control team in Orlando. The successful candidate will be responsible for performing analytical testing on raw materials, in-process samples, and finished pharmaceutical products to ensure compliance with established quality standards and regulatory requirements. This is an immediate opening for a dedicated professional eager to contribute to the quality assurance of life-saving medications.
Key Responsibilities
- Perform routine and non-routine analytical testing of raw materials, in-process samples, and finished products using various analytical techniques (HPLC, GC, UV-Vis, FTIR, wet chemistry).
- Document all analytical data and results accurately and completely in accordance with cGMP regulations and internal SOPs.
- Calibrate and maintain laboratory instrumentation to ensure proper functioning and data integrity.
- Investigate out-of-specification (OOS) results, identify root causes, and implement corrective actions.
- Develop and validate new analytical methods or improve existing ones as needed.
- Participate in laboratory audits and inspections, ensuring compliance with regulatory guidelines (FDA, ICH).
- Adhere to all safety guidelines and maintain a clean and organized laboratory environment.
Required Skills
- Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific field.
- Minimum of 2 years of experience in a Quality Control laboratory within the pharmaceutical or biotechnology industry.
- Proficiency in cGMP, GLP, and pharmacopeial requirements (USP, EP, JP).
- Demonstrated expertise with analytical techniques such such as HPLC, GC, UV-Vis, and FTIR.
- Strong understanding of data analysis and statistical process control.
- Excellent written and verbal communication skills.
- Ability to work independently and as part of a team in a fast-paced environment.
Preferred Qualifications
- Master's degree in a relevant scientific discipline.
- Experience with LIMS (Laboratory Information Management System) and electronic documentation systems.
- Previous experience with method development and validation.
- Knowledge of stability testing protocols.
Perks & Benefits
- Comprehensive health, dental, and vision insurance plans.
- 401(k) retirement plan with company match.
- Paid time off, including vacation, sick leave, and holidays.
- Life and disability insurance.
- Employee assistance program.
- Tuition reimbursement and professional development opportunities.
- On-site fitness center and wellness programs.
- Performance-based bonuses.
How to Apply
If you are interested in this position, please click the "Apply Now" button below. To ensure your application is properly considered, please prepare the following:
- An up-to-date Resume or CV
- A brief cover letter summarizing your experience and motivation
Applications are reviewed on a rolling basis. Only shortlisted candidates will be contacted for an interview.
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