Qureos Mentor

BPI labs (Belcher Pharmaceuticals LLC)

Job SummaryWe are seeking a driven, enthusiastic individual looking to jumpstart a career in the pharmaceutical manufacturing industry. The Trainee Chemist will be analyzing pharmaceutical raw materials, process intermediates and finished product stability samples while following approved standard test methods and procedures.Responsibilities:<ul><li>Develop analytical methods under supervision.</li><li>Validate analytical methods under supervision.</li><li>Analyzes pharmaceutical raw materials, process intermediates and finished product stability samples following approved standard test methods and procedures.</li><li>Performs Chemical analysis work under supervision.</li><li>Documents the testing sequences of steps results as per STMs and SOPs.</li><li>Calculate and interprets test results as per test methods and specifications.</li><li>Notifies supervisor of out of specification (OOS)/Out of Trend (OOT) test results.</li><li>Operates, maintains, and calibrates equipment in assigned area.</li><li>Performs work related assignments as required by management.</li><li>Reviews documentation.</li><li>Follows safety rules.</li><li>Conducts basic troubleshooting of equipment.</li><li>Coordinates as required the maintenance of lab equipment.</li></ul>Qualifications:<ul><li>Master&rsquo;s or PhD in Pharmaceutical Sciences or Analytical Chemistry, or related field.</li><li>Hands-on experience with advanced analytical instruments such as UPLC, GC, GC-MS, Zetasizer, SEC-MALLS, and Ion Chromatography.</li><li>Knowledge of analytical method development, validation, and troubleshooting is preferred.</li><li>Familiarity with regulatory requirements (e.g., ICH, USFDA) is a plus.</li><li>Strong problem-solving skills and ability to work independently and in a team.</li><li>Excellent written and verbal communication skills with attention to detail.</li></ul>Job Type: Full-timePay: $47,483.61 - $57,184.56 per yearBenefits:<ul><li>401(k)</li><li>Dental insurance</li><li>Employee assistance program</li><li>Health insurance</li><li>Paid time off</li><li>Vision insurance</li></ul>Work Location: In person

Trainee Chemist

We are seeking a motivated and talented Process Engineer to join our team in developing and manufacturing lifesaving sterile drug products such as pre-filled syringes, vials, cartridges and autoinjectors. The Process Engineer plays a critical role in designing, scaling up, and optimizing manufacturing, labeling, and packaging processes in compliance with current Good Manufacturing Practices (cGMP).The Process Engineer will work with advanced equipment including automated/robotic fillers, filtration and purification systems, sterilizers, isolators, and supporting utilities such as HVAC, steam, compressed air, and USP-quality water systems. The role also involves troubleshooting, process improvement, and collaboration with vendors and cross-functional teams.Responsibilities:<ul><li>Design facilities, process equipment, and utilities to support next-generation medicinal products and technologies.</li><li>Attend review meetings; review and approve user requirement specifications, design specifications, functional specifications, and qualification protocols.</li><li>Attend Factory Acceptance Tests (FAT) to ensure equipment and machinery perform as expected.</li><li>Support formulation, manufacturing, filtration, sampling, and in-process testing of sterile drug products using advanced equipment and instruments.</li><li>Set up, operate, and validate sterile fill robots, automation systems, and software.</li><li>Operate, maintain, and validate mixing equipment such as magnetic drive mixers.</li><li>Collaborate with formulation scientists on drug development and experimental design.</li><li>Define and control critical process parameters to ensure consistent product quality.</li><li>Develop manufacturing processes to eliminate contamination and ensure product safety.</li><li>Operate and validate steam sterilizers and perform sterilization qualification studies.</li><li>Prepare and review regulatory submissions (NDAs/ANDAs and CMC Module 3).</li><li>Design and validate terminal sterilization processes.</li><li>Ensure all critical activities comply with SOPs, protocols, and regulatory standards.</li></ul>Qualifications: <ul><li>Bachelor&rsquo;s degree in Chemical Engineering, Pharmaceutical Engineering, or Pharmacy with an engineering background.</li><li>Strong verbal and written communication skills with attention to detail.</li><li>Ability to work independently and collaboratively in a team-oriented environment.</li><li>Skilled in troubleshooting equipment and performing complex system tests.</li><li>Familiarity with automation, motion control, pneumatics, and reading P&amp;IDs and schematics.</li><li>Willingness to work in a GMP manufacturing environment, including aseptic cleanrooms and shift operations.</li><li>Eagerness to learn and adapt to new technologies and workflows.</li></ul>Job Type: Full-timePay: From $50,000.00 per yearBenefits:<ul><li>401(k)</li><li>Dental insurance</li><li>Employee assistance program</li><li>Health insurance</li><li>Paid time off</li><li>Vision insurance</li></ul>Work Location: In person

Process Engineer

Join BPI labs (Belcher Pharmaceuticals LLC) and explore 2   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

BPI labs (Belcher Pharmaceuticals LLC)

ABOUT_COMPANY

Trainee Chemist

Process Engineer