Pharmaceutical Manufacturing Process Technician

Transpire Bio; Weston (FL); On-site; USD 39,000 - 50,000; Full time

Job summary

An established industry player is seeking a dedicated Pharmaceutical Manufacturing Process Technician to join their team. This role involves conducting laboratory activities, including manufacturing process development and scale-up, while adhering to regulatory guidelines and industry best practices. The ideal candidate will possess extensive experience in pharmaceutical manufacturing, particularly with solid dosage forms. Join a collaborative environment where your contributions will significantly impact the development of innovative drug products. If you are passionate about making a difference in the pharmaceutical industry, this opportunity is perfect for you.

Qualifications

• 5+ years of experience in a manufacturing technician role in pharmaceuticals.
• Ability to follow health and safety regulations and SOPs.

Responsibilities

• Conduct lab activities including manufacturing process development and scale-up.
• Execute manufacturing batch records and report activities according to cGMPs.

Skills

Pharmaceutical Manufacturing Experience

Problem-Solving Skills

Multitasking Ability

Mathematical Skills

Communication Skills

Education

High School Diploma

Relevant Degree or Certification

Tools

MS Office

Job description

Pharmaceutical Manufacturing Process Technician

Pharmaceutical Manufacturing Process Technician

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NOTE: This role does NOT offer visa sponsorship or visa transfer for work authorization. External applicants must be eligible to work in the US.

Job Summary

Conducts laboratory activities including manufacturing process development, manufacturing process scale-up and process transfer activities across equipment, manufacturing scales and sites. Conducts manufacture of lab scale R&D, pilot scale, pivotal scale and commercial scale batches. Contribute towards installation, maintenance and troubleshooting of manufacturing equipment and interface with equipment vendors. Contribute towards development of orally inhaled and nasal drug products (OINDPs) by following regulatory guidelines, industry best practices, US FDA cGMPs, and other relevant guidelines. Contribute towards the development and evaluation of new formulation manufacturing technologies where required.

Essential Duties and Responsibilities

Conducts standard and advanced laboratory activities including manufacturing process development, manufacturing process scale-up and process transfer activities across equipment, manufacturing scales and sites.

Conducts manufacture of lab scale R&D, pilot scale, pivotal scale and commercial scale batches by following written documentation.

Contribute towards installation, maintenance and troubleshooting of manufacturing equipment and interface with equipment vendors.

Contribute towards development of orally inhaled and nasal drug products (OINDPs) by following regulatory guidelines, industry best practices, US FDA cGMPs, and other relevant guidelines.

Contribute towards creation and review of R&D, pilot, pivotal and commercial manufacturing batch records according to cGMPs and Transpire Bio’s SOPs.

Execute manufacturing batch record and report all laboratory and manufacturing activities according to cGMPs and Transpire Bio’s SOPs.

Work and communicate effectively with other functional groups and across global respiratory R&D sites.

Establish and maintain effective relationships with team members.

Conduct lab work in accordance with SOPs; follow Transpire Bio safety rules and procedures.

Comply with all Transpire Bio Corporate guidelines and policies.

Qualification Requirements

THIS ROLE REQUIRES PREVIOUS EXPERIENCE IN A MANUFACTURING TECHNICIAN OR MACHINE/PRODUCTION OPERATOR ROLE IN PHARMACEUTICAL MANUFACTURING

High school diploma with 5 years of work experience.

A relevant degree, certification, or license may be required.

Experience as a technician in the manufacturing of pharmaceutical products.

Experience in the manufacturing of solid dosage forms like tablets, capsules, dry powder inhalation products, is required.

Experience in the manufacturing of sterile, injectables, ophthalmic products is preferred.

A driver's license.

Ability to multitask and liaise with professionals in different fields.

Ability to explain problems simply and clearly.

Proficiency in MS Office.

Exercise independent judgement and discretion.

Ability to understand verbal and written instructions.

Ability to follow health and safety regulations.

Excellent mathematical and problem-solving skills.

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Full-time

Job function

• Job function

  Manufacturing and Production

• Industries

  Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing

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