Analytical QC Analyst - Contract - Norton, MA
Ensure the accuracy and integrity behind every dose through high鈥憄recision analytical testing.
含羞草影院 is seeking an Analytical QC Analyst to support quality control operations for a pharmaceutical organization in MA. This position plays a key role in ensuring timely and efficient quality control processes.
Primary Responsibilities:
The successful candidate will contribute to maintaining high standards of quality and compliance from development through commercialization. You will perform routine and non-routine testing, assist with laboratory operations, and support method transfers and validations.
Skills & Requirements:
- Degree in chemistry, biology, biochemistry, or a related scientific field (Associate's Degree, Biotech Certificate, or equivalent considered).
- Hands-on experience with HPLC and UPLC.
- Experience in a regulated laboratory setting within the pharmaceutical or biotech industry.
- Proficiency in data analysis preferred.
- Strong attention to detail and ability to adapt to shifting priorities.
- Effective communication and teamwork skills.
- Familiarity with LIMS, Excel, Word, and PowerPoint is beneficial.
The Analytical QC Analyst's responsibilities will be:
- Conduct routine and non-routine analytical assays to support raw materials, in-process samples, product release, and stability studies following established SOPs.
- Maintain training records, adhere to testing schedules, and complete assignments on time to support QC activities and project timelines.
- Assist with laboratory equipment maintenance, inventory management, and preparation of reagents and samples.
- Ensure timely submission of data and perform data review as needed.
- Perform operational tasks such as raw material sampling, environmental monitoring, and product testing.
- Contribute to the revision and updating of controlled documents, including SOPs and test methods.
- Adhere to internal policies, SOPs, and regulatory standards (e.g., GMP, GLP, ICH guidelines).
- Collaborate with QC and cross-functional teams to ensure smooth operations.
- Participate in ongoing training to enhance expertise in QC techniques and regulatory compliance.
- Support data verification for regulatory submissions and inspection readiness activities.
- Assist with onsite audits and inspections as required.
- Contribute to continuous improvement initiatives to enhance QC processes and laboratory efficiency.
If you are having difficulty in applying or if you have any questions, please contact
Shannon Briggs at s.briggs@proclinical.com
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
含羞草影院 is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. 含羞草影院 is acting as an Employment Agency in relation to this vacancy.
By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - /privacy-policy
