Porton Pharma Solutions Ltd. is a leading global provider of comprehensive process R&D and manufacturing services to the pharmaceutical industry. We specialize in offering end-to-end solutions for small molecule APIs, dosage forms, and biologics. With a focus on innovation and customer satisfaction, we are committed to delivering high-quality products and services that meet the industry's evolving needs. Our experienced team of experts works tirelessly to ensure every project is completed on time, within budget, and to the highest possible standards. Whether you need support with drug development, manufacturing, or regulatory compliance, Porton Pharma Solutions Ltd. has the expertise and capabilities to help you achieve your goals.

We are seeking an organized and self-motivated Chemical Operations Scientist who will be responsible for providing operational support to our company.

Prerequisites

· BA/BS or equivalent is required.

· Minimum of 2 years of experience in preparative chemistry laboratory and/or manufacturing facilty with preference for cGMP experience.

· Experience within the chemical or pharmaceutical industry is required.

Responsibilities

· Conduct chemical operations and processing activities with a focus on work in non-GMP and cGMP kilo lab(s).

· Conduct chemical operations in small-scale glassware (e.g. 1-5L glass reactors), small scale purification units (e.g. Biotage Isolera or similar system are desirable) in preparation for larger scale manufacturing.

· Maintain Good Documentation Practice.

· Willingness to work with high potency compounds is desirable, but not required.

· Receive, sample, label and ship chemicals and products.

· Assist chemists in non-GMP and cGMP kilo kilo lab(s) with batch set-up, chemical supply staging, preparative chemistry processing, area clean up and vessel clean out.

· Become proficient in all non-GMP and GMP SOPs

· Research production/processing equipment or fixtures for purchase and gathers data relating to their ability to meet organizational needs.

· Develop, maintain and provide training for J-Star personnel on non-GMP kilo lab processes and procedures.

· Manage non-GMP kilo lab equipment reservation, check out, clean out and check in processes.

· Provide overall upkeep, maintenance, organization, and housekeeping of non-GMP and kilo lab suite.

· Dispose waste and empty containers generated from the kilo lab chemical processing activity and direct the J-Star personnel working on non-GMP kilo lab processes to do the same.

· Trouble-shoot, maintain, repair, purchase, replace and install defined kilo lab-related equipment and services.

· Perform cleaning of chemical processing equipment’s and the kilo lab facilities.

· Ensures kilo lab equipment is maintained in good working order

· Coordinate and perform requisite monitoring and record keeping for all chemical-related permits.

· Maintain organized and clean kilo lab facility

· Coordinate kilo lab glassware repair/service with third party provider.

· Perform all job responsibilities with an uncompromising adherence to appropriate PPE utilization.

· Carry out job responsibilities with an uncompromising level of safety and professionalism.

· Complete, understand and acknowledge all J-Star assigned and required training by due dates.

· Follow all company, site and laboratory Environmental, Health and Safety (EHS)-related protocols, processes, guidelines and SOPs. Actively participate in EHS discussions with peers and management for continuous improvement of EHS practices.

· Perform other job-related duties and ad hoc facility-related projects as assigned by manager.

Qualifications

· Proven track record of setting and meeting aggressive targets and timely execution of objectives.

· Excellent written, verbal and communication skills.

· Ability to prioritize and manage numerous projects simultaneously.

· Ability to interact in an effective and appropriate manner with diverse population sets.

· Ability to communicate candidly, clearly and timely.

· Experience in working on, positively contributing to, and leading teams.

· Proficient in Microsoft®Office™and other job-related software and applications.

· Ability to perform the physical requirements of the position. Must be able to walk, stand, crawl, stoop, crouch, bend or reach above and below shoulders height frequently. This job requires twisting and turning of the body and the use of both hands

Job Type: Full-time

Benefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Health insurance
• Health savings account
• Life insurance
• Paid time off
• Vision insurance

Schedule:

• 8 hour shift
• Monday to Friday

Education:

• Bachelor's (Preferred)

Experience:

• CRO: 4 years (Preferred)
• chemical production work/chemistry laboratory: 4 years (Required)
• GMP HPAPI LAB: 2 years (Preferred)

Ability to Relocate:

• Cranbury, NJ 08512: Relocate before starting work (Required)

Work Location: In person