QC Chemist

ANI Pharmaceuticals•Baudette, MN

2d•$48,000 - $52,000•Onsite

About The Position

Welcome to ANI Pharmaceuticals, where we are dedicated to improving and enhancing patients' lives through the manufacturing and distribution of high-quality pharmaceutical products. With a diverse portfolio of generic and branded pharmaceuticals, ANI is a trusted partner for healthcare providers, pharmacists, and patients alike. We understand the importance of accessibility, and our products are available across a wide range of therapeutic areas, contributing to the well-being of communities globally. At ANI Pharmaceuticals, there are opportunities to contribute to our purpose every day. We value authenticity, knowledge, and hard work, we strive to celebrate our employees in a positive environment. Our culture empowers everyone to be successful and apply our full potential.

Requirements

Bachelor's degree in Chemistry or closely related field/major.
2 - 5 years experience in an analytical chemistry lab in a Pharmaceutical or similarly regulated environment
Ability to work independently
Demonstrated expertise of Laboratory cGMPs
Follow written procedures and perform technical writing.
Organization, communication and interpersonal skills.
Ability to carefully handle fine glassware, sampling devices and perform data entry
Ability to lift up to 20 lbs.

Nice To Haves

Post graduate education in the field of Chemistry, Pharmacy, or closely related field.
1 year of experience in ANI Pharmaceuticals analytical lab, and/or experience in testing methodology.
3 - 5 years experience in an analytical chemistry lab in a Pharmaceutical or similarly regulated environment.
Experience developing lab procedures and systems preferable in a pharmaceutical or similarly regulated environment.

Responsibilities

Perform laboratory testing on material and product samples.
Prepare standards and samples in accordance with approved procedures.
Set-up and confirm suitable operation of equipment and instrumentation.
Collect data and generate/report results in accordance with governing test methods and SOPs.
Report discrepancies, and assist/mentor peers.
Perform review of data collected under approved test methods and investigational plans and protocols, in accordance with governing SOPs.
Provide accurate assessment of data integrity, and document findings.
Work with peers to correct deficiencies, and assure understanding.
Perform calibration, preventive maintenance, and repair as needed on assigned equipment.
Update equipment procedures to reflect proper usage and maintenance.
Perform cGMP tasks as assigned such as monitor expiry dates, auditing documentation and logbooks, and ordering supplies.
Prepare PPA's, investigation reports, and Method/SOP/IOP revisions.
Performs other duties as assigned or requested.