Chemist C
Acrotech Biopharma Inc · Dayton, NJ · 2 days ago
On-siteAnalyst$85k/yrFull-time
Job Overview
The Chemist-C will perform a variety of QC testing to assess the strength, identity, and purity of test samples and/or materials. They will work as a member of a team to effectively plan and QC analytical testing using established (official and/or in-house) test procedures.
Responsibilities
- Perform assigned sampling, physical, chemical tests and assays on raw materials, active pharmaceutical ingredients, in-process, finished and stability products, using various wet chemicals, physical and instrumental techniques (HPLC, GC, UV-Vis, IR, Particle Size Analyzer, KF Auto titrator, Bulk Density, and other routine QC instruments) as per USP monograph / In-house / any other Compendial monographs.
- Independently plan and make adequate inventory of test reagents and solutions to perform work, assure supplies are ordered as needed to perform assigned work.
- Independently plan and execute testing to meet established time lines.
- Perform complicated testing with supervisory direction.
- Record data and results as specified in documentation procedures.
- Document work clearly and perform tests accurately.
- Prepare and/or Review Test Procedures, SOPs, and Protocols as assigned.
- Perform maintenance and calibrations of laboratory instruments/equipments with supervisory direction/training.
- Perform troubleshooting and investigations under the direction of a supervisor.
- Comply with all regulatory/in-house requirements (may include but not limited to safety, house keeping, laboratory chemical waste, cGMP, cGLP, documentation) when performing the assigned activity.
- Review of Analytical documents as required.
- Active involvement in training and qualification of newly hired chemists.
- Be a role model and mentor to lesser experienced analysts in the team.
Qualifications & Requirements
- Knowledge in Good Documentation practices.
- Knowledge in USP/ICH/FDA.
- Ability to learn quickly and decision making skills.
- Attention to detail and documentation.
- Proficient in working with Empower and LIMS.
- 2-4 years of experience with handling Out Of Specification investigations.
Education & Experience
- Minimum BS within Scientific field, BS with Chemistry is preferable.
- Minimum 4-6 years experience in pharmaceuticals and must have 3-5 years experience in Analytical testing.
- 3 years QC experience in Generic Pharmaceutical industries is preferable.
Benefits
- Medical and Rx Benefits choice of four medical plans through Horizon. Rx automatically provided with medical benefits.
- Dental Benefits with three dental plan options through CIGNA.
- Vision Plan with two plan options through VSP.
- Life Insurance, Basic Life and AD&D and Supplemental Life Insurance.
- Disability Insurance, Voluntary Short-Term Disability and State Disability Long-Term Disability (LTD), State (short term) disability – where applicable.
- FSA (Flexible Spending Accounts) – Both Health Care & Dependent Care Available.
- HSA (Health Savings Account).
- 401(k) Plan - Through Fidelity / Employer Match / fully vested after 3 years.
- Employee Assistance Program (EAP) - 100% Confidential and 100% company paid.
- Critical Illness and Accidental Insurance.
- Legal and Identity Theft Insurance.
- Paid Time Off - Paid vacation, PTO, Holiday Notice.
Compensation
Min USD $85,000.00/Yr. Max USD $90,000.00/Yr.
Physical Requirements
- Work in a temperature controlled office environment or travel via vehicle or commercial transportation.
- Occasionally handle or feel objects, talk, hear, and walk during the course of employment.
- Some degree of travel for business purposes.
- Lifting 8+ Hours - 0-10 Pounds.