Join The JSP Family

JSP strives to bring the most for it’s employees and continues to offer some of the most competitive benefits package in the industry including competitive salaries and bonus. Career opportunities offering both personal and professional growth.

4-Day Work Week

JSP employees enjoy a 4-Day Work Week (Monday - Thursday) on a single shift 7:30am - 6:00pm

Jerome Stevens Pharmaceuticals, Inc. is unable to accommodate hybrid/remote work

Benefits

401 (K) Plan that includes a 3% “Safe Harbor” contribution; profit sharing for your retirement plan; comprehensive medical and dental plans that provide coverage for you and your.

Medical & Dental Benefits for you and your family

Competitive Salary, Accrued Sick and Vacation Time

Annual Bonus

 
 

COMPRESSION SETUP MECHANIC — Bohemia, NY

Jerome Stevens Pharmaceuticals, Inc. is seeking experienced hardworking, honest candidates for a Tablet Press Mechanic position in the Compression and Encapsulation Department.

Job Requirements:

  • Experience in FDA-regulated environment, minimum 2-years

  • Hardworking and Attentive to Detail

  • Familiar with cGMP and SOP’s

  • Experience with Compression machines such as Fette 3090 and 2200

  • Experience with Encapsulation machines such as IMA Matic – 90

  • Experience with Rotary Tablet Press machines such as Korsch XL400_4 SFP

  • Ability to follow instructions carefully

  • Excellent written and verbal communication skills

  • Strong attention to detail

  • Computer experience, a plus

  • Ability to read and comprehend company procedures and policies (be advised, all company documentation is in English)

PHARMACEUTICAL PURCHASER — Bohemia, NY

Jerome Stevens Pharmaceuticals, Inc. is seeking a hardworking, detail-oriented, and experienced Pharmaceutical Purchaser for Company procurement, shipping/receiving, and inventory control activities.

Job Requirements:

  • Proficient in MS Office Suite (Outlook, Word, Excel) and Quickbooks Enterprise

  • Experience in MS Dynamics, a plus

  • Min. 3-year pharmaceutical industry experience

  • Ability to write, speak and interact clearly and professionally

  • Extremely organized. Strong follow-up ability, multi-tasking and time-management skills

  • Persistent and self-starter – working with minimal supervision.

  • Can handle sensitive information with the highest degree of integrity and confidentiality

  • Familiarity with both Mac and PC environments

  • Current and proficient in trends, concepts, technologies, and best practices within profession

 

TECHNICAL OPS SUPERVISOR — Bohemia, NY

Jerome Stevens Pharmaceuticals, Inc. is seeking a hardworking, detail-oriented, and experienced Technical Operations Supervisor for Company research & development and GMP production initiatives with experience in process validation, qualification, and regulatory filings.

Job Requirements

  • Experience with FDA submissions including new product approval and post-approval change applications

  • Detailed knowledge of drug product manufacturing floor activities

  • Experienced with use of statistics to analyze process related data

  • Strong hands-on cGMP and FDA regulatory and SOP knowledge

  • Proficient in MS Office Suite (Outlook, Word, Excel)

  • Master’s degree in chemical engineering or pharmaceutical engineering with minimum of 2 years of directly related experience in a Technical Services function within the Pharmaceutical industry or a bachelor’s degree in chemical engineering or pharmaceutical engineering with minimum of 4 years of directly related experience in a Technical Services function within the Pharmaceutical industry

  • Advanced knowledge of the standards and concepts applicable to a wide range of work in pharmaceutical dosage processing including the areas of tech transfer, commercial manufacturing, and unit operations

  • Hands on experience in commercial drug product manufacturing/packaging equipment and processes, post-approval change projects and process validation

  • Willingness to travel periodically as needed

  • Ability to write, speak and interact clearly and professionally

  • Extremely organized. Strong follow-up ability, multi-tasking and time-management skills

  • Persistent and self-starter – working with minimal supervision.

  • Can handle sensitive information with the highest degree of integrity and confidentiality

  • Familiarity with both Mac and PC

  • Current and proficient in trends, concepts, technologies, and best practices within profession

SENIOR QUALITY CONTROL ANALYST — Bohemia, NY

Jerome Stevens Pharmaceuticals, Inc. is seeking to hire full-time Quality Control Analysts with High Performance Liquid Chromatography (HPLC) and Solid Oral Dosage experience at our Long Island facilities.

Job Requirements

  • Carries out responsibilities in accordance with the organization’s policies, procedures, and state, federal and local laws

  • Performs more complex chemistry testing

  • Operates general analytical instruments during release testing (i.e., HPLC, UV, IR)

  • Performs wet Chemistry tests on raw materials as required by USP (i.e., LOD, pH, KF, etc.)

  • Prepares standard and sample solutions as required by test methods

  • Maintains appropriate documentation (records and lab notebooks) as required by company procedures

  • Complies with all current Good Laboratory Practices (cGLP), current Good Manufacturing Practices (cGMP) and safety requirements, laboratory Standard Operating Practices (SOPs) and Company policies and procedures

  • Participates in troubleshooting and review of analytical test methods and laboratory instruments

  • Perform analysis on intermediate product, finished product, and stability samples