Engineer I - Manufacturing Science and Technology

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.

We are PCI.

Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.

The Manufacturing Technical Specialist provides technical (scientific / engineering) knowledge to enable GMP manufacturing, ensure regulatory compliance, inclusive of direct client support. These efforts are directed to support the company's Aseptic and Non-Aseptic manufacturing processes including Pharmaceutical Form / Fill / Finish and Medical Device manufacturing. At level I, the MTS Specialist receives guidance and direct supervision in the execution of their duties. The Specialist I assists in the technical transfer of client processes, generate batch records and reports for technical studies, and provide Quality System support via the ownership of deviations, CAPAs, change controls, and excursion investigations. The incumbent is also expected to support efforts to develop, edit, and complete additional GMP documentation (e.g., SOPs, material specifications, training documentation) related to manufacturing operations and client specifications. The Manufacturing Technical Specialist is engaged in providing input and feedback for the PCI Safety Program to meet health and safety regulations and OSHA requirements.

Essential Duties and Responsibilities : To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The essential duties and responsibilities include the following but other duties may be assigned.

With supervision and guidance, provide technical support to project management and manufacturing operations during the technical transfer of new processes

Identify and resolve manufacturing issues, improve process operations, and affect positive change

Write batch record modules and SOPs for new processes; perform revisions / edits for existing documents as directed

Assist in specifying equipment, materials, and components with cross-functional groups for new processes

Work with manufacturing operations to develop and maintain production records for safety and compliance

Assist in resolutions to deviations, generate corrective / preventative actions, (and support Quality documentation for manufacturing processes

Perform root cause analysis for investigations; perform risk assessments when required

Meet and interact with clients from the initiation of technical transfer, during the manufacturing process, and following operations, providing technical knowledge and expertise at every stage of the project

Perform other duties as required to support PCI operations

Works directly with aseptic, non-aseptic, and medical device Operations personnel and Project Management Leads. Works closely with Quality Assurance, Validation, EHS, Engineering, Facilities and will directly interface with clients

Special Demands : The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. The employee must be physically capable to perform the duties listed below with or without reasonable accommodations which may be made to enable individuals with disabilities to perform the essential functions.

Ability to wear personal protective equipment such as safety glasses / goggles, gloves and safety shoes

Ability to gown and gain entry to controlled manufacturing areas

Ability to lift, pull or push equipment requiring up to 25 lbs. of force

Ability to stand for prolonged periods in a production suite and work extended hours as needed

Work Environment : The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Qualifications : The requirements listed below are representative of the knowledge, skill, and / or ability required for the stated position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

• Bachelor's or associate degree in life sciences or related discipline with One + years' experience in a technical, quality, or manufacturing role required, 2+ years of GMP experience in a regulated industry (e.g., pharmaceutical, biotech, or medical device) preferred. Comparable blends of education and / or experience is acceptable.

Knowledge of Current Good Manufacturing Practices (cGMP), regulatory guidelines, aseptic manufacturing, as well as bulk intermediate and medical device manufacturing

Working knowledge and experience utilizing MS Office (Word / Excel / Access / Visio / PowerPoint)

Clean room (aseptic) experience a plus

Preferred experience with operation of GMP scale manufacturing equipment

Demonstrated proficiency to work in a dynamic, fast paced work environment

Honesty, integrity, respect and courtesy with all colleagues. A team player and contributing collaborator.

Highly effective following through on guidance and work assignments

Flexible and adaptable as the job may require

Professional skills in biopharmaceutical and / or medical product formulation, filtration, and filling operations preferred

Possess excellent problem solving and analytical skills

Skills and knowledge to perform quality system investigations, preferred

Ability to meet aggressive deadlines while multi-tasking

Requires excellent organizational and interpersonal skills

Excellent oral and written communication skills required

Ability to work with supervision and guidance, coupled with the ability to follow through on direction leading to assignment / project completion

Travel

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Equal Employment Opportunity (EEO) Statement :

PCI Pharma Services is an Equal Opportunity / Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

At PCI, Equity and Inclusion are at the core of our company's purpose : Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.

Why work for PCI Pharma Services?

At PCI, we have an uncompromising focus on providing quality and operational excellence and providing the industry leading customer experience. Our people make all of this happen, so providing an industry leading experience for our people is equally as important. By creating an authentic culture of purposeful work, we aspire to be an interesting and fulfilling place for talented individuals to grow careers. We live a philosophy of intentional learning combined with real-life experience supported by a fair and competitive rewards program. We are individuals, teams and a company that believes in our purpose and our approach is simple, the people who work at PCI fuel our business; we don't say no, we figure out how.

PCI Pharma Services is an Equal Opportunity Employer / Vet / Disabled