At a Glance
- Tasks: Conduct analytical testing and ensure the quality of life-changing pharmaceutical products.
- Company: Leading pharmaceutical company with a commitment to quality and innovation.
- Benefits: Competitive salary, health coverage, generous PTO, and remote work flexibility.
- Other info: Join a supportive virtual team and enjoy professional development opportunities.
- Why this job: Make a real impact on patient well-being from the comfort of your home.
- Qualifications: Bachelor's or Master's in Chemistry with 4+ years in quality control.
The predicted salary is between 82800 - 101200 $ per year.
About the Role
Our client, a leading pharmaceutical company committed to the highest standards of quality, is seeking a skilled Senior Pharmaceutical Quality Control Analyst to join their fully remote team.
This position offers the flexibility to work from anywhere, contributing to the critical analysis and testing of pharmaceutical products to ensure their safety, efficacy, and quality.
You will perform a variety of analytical tests, interpret results, and contribute to method development and validation.
The role requires a deep understanding of analytical chemistry techniques, laboratory practices, and regulatory requirements within the pharmaceutical industry.
The ideal candidate is highly detail-oriented, proficient with analytical instrumentation, and capable of working independently in a virtual setting.
This is an exceptional opportunity for an experienced analyst to advance their career while contributing to the development of life-changing medicines from the convenience of their home environment.
Embrace a career where your analytical expertise directly impacts patient well-being.
Key Responsibilities
- Perform analytical testing on raw materials, in-process samples, and finished products using various instrumental techniques (e. g., HPLC, GC, UV-Vis, FTIR).
- Analyze and interpret test results, ensuring accuracy and compliance with specifications.
- Document all laboratory activities meticulously in accordance with GMP guidelines.
- Participate in the development, validation, and transfer of analytical methods.
- Operate and maintain laboratory equipment, ensuring calibration and readiness.
- Troubleshoot analytical methods and instrumentation issues.
- Prepare certificates of analysis and contribute to quality control reporting.
- Review data generated by other analysts for accuracy and completeness.
- Stay updated on relevant scientific literature and regulatory guidelines.
- Contribute to laboratory investigations and CAPA resolutions.
Requirements
- Bachelor's or Master's degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or a related field.
- Minimum of 4 years of experience in pharmaceutical quality control or analytical development.
- Proven experience with HPLC, GC, and other common analytical techniques.
- Strong understanding of GMP principles and regulatory requirements.
- Experience with method validation is highly desirable.
- Excellent data interpretation and problem-solving skills.
- Exceptional attention to detail and organizational abilities.
- Strong written and verbal communication skills, essential for remote collaboration.
- Ability to work independently and manage workload effectively in a remote setting.
- Proficiency in LIMS and electronic data management systems is a plus.
Benefits
- Competitive salary and annual bonus structure.
- Comprehensive health, dental, and vision insurance coverage.
- Generous paid time off and company holidays.
- Retirement savings plan with employer matching.
- Professional development opportunities, including training and certifications.
- Fully remote work arrangement with a home office setup stipend.
- Access to advanced digital collaboration platforms.
- Opportunity to work with a leading pharmaceutical company.
- Flexible working hours.
- A supportive and collaborative virtual team environment.
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