Senior Quality Control Analyst I (GC)

Senior Quality Control Analyst I (GC)

On-siteQC AndoverFull time1646

Andover, Massachusetts, United States

Description

Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Senior Quality Control Analyst I based onsite in our Andover, MA facility. CIL is the global leading company in a highly technical, extremely fast-growing industry and is a critical supplier to several scientific and high technology markets. CIL's growing customer base spans academia, pharmaceutical, medical diagnostic and semiconductor industries enabling collaborations with Nobel laureates, industry-leading scientists, and chemists. CIL partners with leading instrument manufacturers as well pioneering research groups that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years.

The Senior Quality Control Analyst I is responsible for providing direction, guidance and training to QC Analysts on, as well as independently performing, the following: routine and non-routine analysis of GMP and ISO materials in accordance with standard operating procedures (SOPs). The Senior QC Analyst I is able to perform method validations and troubleshoot issues in at least one area of expertise. They also compile data for documentation of test procedures and prepare reports, as well as calibrate and maintain lab equipment. They may also provide input to QC Management for QC Analysts' performance reviews as requested. Occasional travel between facilities may be required.

Responsibilities

Responsible for performing tests and/or calibrations and evaluations or results related to GMP and ISO materials and products as appropriate

Perform or direct, guide and train others to perform the following:

Follow documented procedures

Document test data as required

Utilize one or more of the following techniques to characterize organic and inorganic chemicals: FT-NMR, LC/MS, GC/MS, GC, HPLC, FT-IR and wet chemistry tests

Write/develop test procedures as required

Calibrate, maintain, and troubleshoot laboratory equipment

Acts as a subject matter expert in at least one area of analytical techniques

Provide input to QC Management for QC Analysts' performance reviews as requested

Additional functions may be assigned

Requirements

Bachelor's degree in Chemistry or a related field with at least 5+ years of industry lab experience, OR a Master's degree in Chemistry or a related field with at least 3+ years of industry lab experience, OR a PhD in Chemistry or related field with 1-3 years of industry lab experience

Experience with GC, GC/MS, NMR, HPLC or LC/MS required; QC experience preferred

Experience with GMP, ISO 9001, ISO 13485, or ISO 17034 a plus

Hands-on experience with Biovia ELN/LIMS preferred; Cheminformatics experience a plus

Must be able to multitask in a fast-paced environment and possess strong verbal and written communication skills

Must be able to work effectively independently and as part of a team

Must be comfortable handling various chemicals and gases in a laboratory setting

Must be able to travel between the Tewksbury, MA and Andover, MA facilities

Benefits

CIL and CIS offer a competitive salary and comprehensive benefits including generous paid time off, Long Term Incentives, 6% matching 401K plan and health insurance with no in-network deductible.

Cambridge Isotope Laboratories is an Equal Opportunity Employer.