Chemist

A brief overview The role of the Chemist is to manufacture active pharmaceutical ingredients (APIs) and perform related activities within a cGMP regulated environment. What you will do Install, operate and maintain equipment for manufacturing and in‑process testing (HPLC/UPLC, lyophilizers, balances, reactors, HF cleavage equipment, diafiltration systems, water purification systems, ovens, washing systems, etc.) Perform solid phase and liquid phase synthesis, deprotect and cleave the API from the resin using chemical cocktails containing HF, TFA, ammonium hydroxide or other chemicals Perform purification via chromatography, crystallization and other techniques Follow approved GMP manufacturing directions such as Master Batch Records, Standard Operation Procedures, Standard Test Procedures and other procedures to manufacture GMP materials, perform in‑process tests, package the product and related activities Plan projects and initiate raw material orders. Receive raw materials, coordinate with QA/QC and Material Management for release and monitor inventories Maintain GMP Documentation System; investigate deviations and produce reports; initiate document change requests; assist QA/QC with equipment calibration programs Maintain and organize work areas (hood, bench, floor, wall, etc.) and other designated areas within the manufacturing facility Write and improve Standard Operation Procedures (SOPs), Standard Test Procedures (STMs), Master Batch Records (MBRs) and other related GMP documents Clean equipment used in GMP processes, maintain cleaning logs, assist in calibration programs, and dispose of chemical waste generated during manufacture Monitor compliance of maintenance and cleaning procedures for equipment and instruments by reviewing and signing off maintenance and cleaning logs Qualifications Bachelor’s degree in chemistry or related field (or 10+ years of relevant experience) Experience in GMP manufacturing and basic knowledge of cGMP and FDA regulations (preferred) Experience in the manufacture of peptides and oligonucleotides (preferred) Capable of following GMP guidelines and housekeeping rules Excellent written and oral communication skills Effective teamwork and proactive problem‑solving skills Flexibility of working hours, may include occasional nights or weekends based on business needs Ability to work independently and manage one’s time Ability to organize, multitask and work in a fast‑paced, deadline‑driven environment Detail‑oriented with problem‑troubleshooting skills Basic computer knowledge (Microsoft Word, Excel, PowerPoint) Ability to work safely with hazardous materials and chemicals Base Hourly Ranges Placement of new hires in these wage ranges is based on several factors including education, skill sets, experience, and training. Total Rewards Compensation includes competitive pay, an annual performance bonus, a comprehensive benefits package (Medical, Dental, Vision), a 401(k) plan with employer contribution, and paid vacation, personal and sick days. Equal Opportunity Employer Bachem Americas is an Equal Opportunity Employer. As an equal opportunity employer, we celebrate the diversity of our team and are committed to building an inclusive workplace where individuals are hired and advanced based on merit, skills, and qualifications. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status, or other legally protected status. #J-18808-Ljbffr