Quality Control Analyst III

Curia Aalborg ApS; City of Rensselaer (NY); On-site; USD 84,000 - 95,000; Full time

Benefits offered by this job

Benefit options

Paid training

Career advancement

Education reimbursement

401K match

Learning platform

Job summary

Curia is hiring a Quality Control Analyst III in Rensselaer, NY for day shift. The role supports manufacturing and external customers with testing of raw materials, in-process, end products and stability samples.

Responsibilities include performing TGA and LC/UPLC analysis, assisting with test method validations, data trend evaluation, OOS investigations, CAPA, and preparation of SOPs and data summaries. A strong GMP/regulatory background is preferred.

Qualifications

• Bachelor's degree in Chemistry or related field.
• Minimum 5-7 years pharmaceutical experience or equivalent combination of education and experience.

Responsibilities

• Perform complex testing and data evaluation (e.g., TGA).
• Conduct LC/UPLC testing and troubleshoot as needed.
• Support OOS investigations and CAPA requirements.
• Prepare data summaries and trend evaluations.
• Lead or participate in cross-department meetings and projects.

Skills

TGA testing

LC/Chromatography

Data evaluation

CAPA investigations

Regulatory knowledge

Education

Bachelor's degree in Chemistry

Tools

TGA instrument

UPLC

GC/LC

Job description

Job Description

Quality Control Analyst III in Rensselaer, NY - Day shift

Our Rensselaer site is undergoing a crucial quality transformation. This is a rare opportunity to join a highly visible project, re‑engineer quality systems from the ground up, and gain unmatched regulatory exposure. Build your future at Curia, where our work has the power to save lives

Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life‑saving treatments to patients. At Curia, we are on a mission to advance our customers’ therapies from curiosity to cure and ultimately to improve patients’ lives.

We proudly offer

• Generous benefit options (eligible first day of employment)
• Paid training, vacation and holidays (vacation accrual begins on first day of employment)
• Career advancement opportunities
• Education reimbursement
• 401K program with matching contributions
• Learning platform
• And more!

Position overview

The Quality Control Analyst III is responsible for supporting the manufacturing department and external customers. Routine functions include testing of raw materials, in-process, end product, and stability samples.

Essential Job Duties

• Perform complex testing and data evaluation such as TGA
• Perform complex Liquid/Gas Chromatography, UPLC, and other testing, and, as needed, troubleshoot issues
• Participate in or assist with test method validations
• Evaluate data for trends
• Support supervisors in OOS Investigations and complete CAPA requirements
• Interact with outside departments including attending meetings, providing updates, etc.
• Coordinate testing performed at outside testing labs, raw materials, etc.
• Maintain a detailed and accurate recording of activities and results on paperwork
• Execute, author, and review SOPs, reports, protocols, investigations, change controls, and data summaries. Understand and use basic risk assessment and root cause tools
• Train upon and understand methods, equipment and standard operating procedures
• Provide training to others as needed. Attend internal and external training on related subjects, including both intra- and inter‑departmental cross‑training on new techniques and procedures
• Support equipment upkeep and laboratory method trouble shooting
• Provide technical assistance during the shift for test method trouble shooting
• Prepare and order supplies, as necessary
• Enter data into relevant data management systems. Perform tracking and trending of data as requested. Compile data and provide data summaries to management
• Utilize a thorough understanding of regulatory and compliance guidelines for the pharmaceutical industry
• Interact with other departments within the company for testing needs and scheduling
• May lead departmental projects with the opportunity to participate in or lead cross‑functional teams, including continuous improvement projects and new customer teams
• May lead stability program including management of test points, reporting of data, and investigations of out of specification or aberrant stability results

Required - Education, experience, certification and licensures

• Bachelor's degree in Chemistry or related field
• Minimum 5-7 year’s pharmaceutical experience or equivalent combination of education and experience

Preferred

• Experience working in cGMP or GLP pharmaceutical industry environment

Knowledge, Skills And Abilities

• Excellent verbal and written communication skills, including the ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public
• Ability to meet deadlines and work under pressure with limited supervision
• Strong time management and organizational skills with the ability to multi-task and manage multiple projects independently
• Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations
• Ability to write reports, business correspondence, and procedure manuals
• Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations
• Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis
• Ability to define problems, collect data, establish facts, and draw valid conclusions
• Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables
• Proficient use of computer software, including Microsoft Office Suite and instrument manufacture-based systems
• Knowledgeable in FDA GMPs (21 CFR, 211, 820, and or 600); ISO 9001 and 13485 a plus

Pay Range

$84,000 - $95,000

Education, experience, location and tenure may be considered along with internal equity when job offers are extended.

Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E-Verify employer.