Job Title: Quality Control (QC) Analyst
Location: Texas, USA
Company: A leading Contract Development and Manufacturing Organization (CDMO)
The Company:
My client are dedicated to providing exceptional contract development and manufacturing services to the pharmaceutical and biotechnology industries. Their state-of-the-art facilities in Texas are equipped to handle the most demanding projects, ensuring the highest quality standards are met. Join the team and contribute to our mission of delivering life-changing therapies to patients around the world.
Position Summary:
We are seeking a highly skilled and motivated Quality Control (QC) Analyst to join the team. The QC Analyst will play a critical role in ensuring the quality and compliance of our products by performing a variety of laboratory tests and analyses. The ideal candidate will have a strong background in analytical chemistry and a keen eye for detail.
Key Responsibilities:
- Conduct routine and non-routine analysis of raw materials, in-process samples, and finished products using techniques such as HPLC, GC, FTIR, UV-Vis, and other analytical methods.
- Perform method development, validation, and transfer activities.
- Maintain accurate and detailed records of all laboratory work, including test results, observations, and deviations.
- Ensure compliance with GMP, GLP, and other regulatory requirements.
- Participate in the investigation of out-of-specification (OOS) results and other quality issues.
- Collaborate with cross-functional teams, including R&D, production, and quality assurance, to support project timelines and objectives.
- Assist in the preparation and review of standard operating procedures (SOPs) and other quality documents.
- Maintain laboratory equipment and ensure calibration and maintenance are performed as required.
- Stay current with industry trends, new technologies, and regulatory changes.
Qualifications:
- Bachelor's degree in Chemistry, Biochemistry, or a related field.
- Minimum of 2 years of experience in a QC laboratory within the pharmaceutical, biotechnology, or CDMO industry.
- Proficiency in analytical techniques such as HPLC, GC, FTIR, UV-Vis, and other relevant methods.
- Strong understanding of GMP, GLP, and regulatory guidelines.
- Excellent attention to detail and problem-solving skills.
- Strong organizational and time management abilities.
- Effective communication skills, both written and verbal.
- Ability to work independently and as part of a team in a fast-paced environment.
What my client offers:
- Competitive salary and benefits package.
- Opportunities for professional growth and development.
- A collaborative and inclusive work environment.
- State-of-the-art laboratory facilities.
- The chance to make a meaningful impact on the development and manufacturing of life-changing therapies.
CY Partners is acting as an Employment Business in relation to this position. We are an equal opportunity employer, we celebrate diversity and are committed to creating an inclusive environment for everyone we work with.