Chemist I - Night Shift Job at Piramal Pharma Ltd in Lexington

Overview

The Chemist I performs testing of raw materials, in-process and finished products, and maintains and calibrates analytical instruments in compliance with cGMP standards.

Responsibilities

• Perform routine/non-routine testing, both wet chemistry and instrumental analysis, according to SOPs, testing methods, protocols, compendia (USP EP/JP) with minimum supervision
• Test raw materials, APIs, finished products, stability samples, and cleaning verification samples
• Document laboratory work according to GDP, cGMPs, and SOPs
• Troubleshoot, calibrate and maintain instruments as required
• Prepare and label laboratory reagents, reference standards, or solutions according to SOPs
• Write SOPs, laboratory protocols and reports, memos and/or other interdepartmental correspondence
• Participate in laboratory investigations
• Perform peer review of analytical documentation
• Follow safety procedures when working in the laboratory
• Understand and comply with cGMPs and other regulations
• Maintain the laboratory in an organized and neat manner
• Act as backup for material sampling activities
• Purchasing of laboratory reagents and consumables

Education

• Bachelor of Science in Chemistry, Pharmaceutical Science, or other closely related scientific field

Experience

• Minimum 1-year hands-on experience performing quality control work within a laboratory, proficiency with HPLC/GC analysis strongly preferred
• Experience working with potent, cytotoxic materials and parenteral drug products preferred

Competencies

• High level of proficiency operating all Microsoft Office applications
• Excellent communication skills, both verbally and in writing
• Detail oriented and organized
• Demonstrated ability to work within a team environment, supporting a continuous operation manufacturing facility
• Excellent problem solving, communication, and interpersonal skills
• Ability to follow written instructions

About Us

Piramal Group is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. We also offer specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products. PPS also offers development and manufacturing services for biologics including vaccines, gene therapies, and monoclonal antibodies, made possible through Piramal Pharma Limited’s investment in Yapan Bio Private Limited.

Equal Employment Opportunity

Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics. We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice.