Top 63 Process engineer parenteral Jobs

Sr. Process Engineer
Alcami Corporation —Charleston, SC
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Ability to walk for extended periods
Process Engineer
Piramal Pharma Solutions —Lexington, KY
- $69,000 - $96,000 a year
- Full-time
- Background check
- Microsoft Excel
- 5 years
- Health savings account
- Health insurance
Quick Apply
Manufacturing Process Engineer
Piramal Pharma Solutions —Lexington, KY
- Up to $100,000 a year
- Full-time
- Background check
- Maintenance
- Research
- Health savings account
- Health insurance
Quick Apply
Process Engineer
BioPharma Consulting JAD Group —Carolina, PR
- Contract
- Spanish
- Doctoral degree
- Engineering
Quick Apply
Parenteral Process Scientist or Engineer
Validation & Engineering Group —Municipio de Juncos, PR
- Spanish
- Engineering
- English
Quick Apply
Engineer - Process
Eli Lilly —Indianapolis, IN
- $66,000 - $171,600 a year
- Extended hours
- Mid-level
- Continuous improvement
- Travel
- Health insurance
- Dental insurance
Process Validation Engineer
INCOG BioPharma Services —Fishers, IN
- Full-time
- Engineering
- Office
- Analysis skills
Scientist / Senior Engineer – Drug Product Process Engineering
Amgen —Thousand Oaks, CA
- $111,940.75 - $151,449.25 a year
- 3 years
- Bachelor's degree
- Continuous improvement
- Disability insurance
- Health insurance
Senior Process Engineer
SHARP STERILE MANUFACTURING LLC —Lee, MA
- $90,000 - $140,000 a year
- Full-time
- 3 years
- Ability to lift 50 pounds
- Math
Quick Apply
Packaging Engineer III
Gilead Sciences —Foster City, CA
- $117,895 - $152,570 a year
- Full-time
- 5 years
- Mid-level
- Master's degree
- Health insurance
- Dental insurance
Technical Development Principal Scientist - Computational Biophysics
Genentech —San Francisco, CA
- $120,800 - $224,300 a year
- Online Application
- Computer science
- Computer Science
- Analysis skills
Process Engineer
Piramal Pharma Solutions Inc. —Lexington, KY
- Full-time
- English
- Mid-level
- Continuous improvement
Manufacturing Process Engineer
Piramal Enterprises —Lexington, KY
- Full-time
- Research
- Mid-level
- Windows
Senior Human Factors Engineer
Genentech —San Francisco, CA
- $90,700 - $168,500 a year
- Online Application
- 5 years
- Engineering
- Senior level
Manufacturing Process Engineer
PCI Pharma Services —Bedford, NH
- Overtime
- Computer literacy
- Research
- Analysis skills
Senior Engineer - Process Optimization & Capital Projects
BioPharma Consulting JAD Group —Juncos, PR
- Contract
- Spanish
- Doctoral degree
- Engineering
Quick Apply
Development Engineer
Evonik Industries AG —Birmingham, AL
- Online Application
- 5 years
- Bachelor of Science
- Engineering
- Health insurance
- Life insurance
Sr Engineer
Amgen —Thousand Oaks, CA
- $115,494.60 - $156,257.40 a year
- Doctoral degree
- Engineering
- Master's degree
- Disability insurance
- Health insurance
Sr. Engineer
Weil Group, Inc —Juncos, PR
- Temporary
- Background check
- Spanish
- Computer literacy
Quick Apply
Cleaning Validation Engineer II
Gilead Sciences —La Verne, CA
- $99,705 - $129,030 a year
- Weekends as needed
- Mid-level
- Bachelor's degree
- Continuous improvement
- Health insurance
- Dental insurance

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process engineer parenteral jobs near

Sr. Process Engineer

Alcami Corporation -
Charleston, SC

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Job Details

Full-time

Qualifications

Customer communication
Microsoft Excel
Microsoft Outlook
Word embeddings
Manufacturing facility experience
Pharmaceutical company experience
Pharmaceutical manufacturing facility experience

Full Job Description

At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record.

Are you interested in joining our team?

Job Summary:

The Sr. Process Engineer is accountable for driving results in a fast-paced environment by providing technical support for clinical and commercial parenteral Drug Product manufacturing. The Sr. Process Engineer’s responsibilities include but are not limited to the following: performing tech transfers of new processes and technologies into the site, preparation of documentation to support process validation and batch manufacturing, troubleshooting manufacturing processes, completing process deviations and investigations, and coordinating lab studies with the formulation development lab. These functions will be executed following standard operating procedures and batch records in accordance with FDA and EU requirements and current Good Manufacturing Practices.

On-Site Expectations:

100% on-site position.
1st Shift: Monday - Friday, 8:00am - 5:00pm.

Responsibilities:

Provides technical assistance for process tech transfer and validation efforts for assigned manufacturing projects.
Writes Master Batch Records with a strong understanding of equipment, critical process parameters, in-process tests, etc.
Monitors manufacturing processes during production runs to assess any technical process issues and provides troubleshooting support as needed.
Author manufacturing investigations and complete CAPA assignments.
Composes process validation documentation, including CQA assessment, pFMEA risk assessment, and process validation protocols.
Identifies specific parameters, sampling, and tests used in the validation protocols of new and existing products.
Interact with clients during routinely scheduled project meetings.
Ensures timely completion and compliance with cGMP and all other relevant company training requirements.
Other duties as assigned.

Qualifications:

Bachelor’s degree in Engineering, Pharmacy, or Chemistry.
5 years of experience of technical support in a sterile pharmaceutical manufacturing environment.
Previous experience supporting tech transfer of parenteral Drug Products preferred.

Knowledge, Skills, and Abilities:

Excellent verbal communication, written communication, documentation, negotiation, critical thinking, analytical, problem solving, detail orientation, organization and time management skills required.
Working knowledge of cGMP requirements related to sterile Drug Product manufacturing processes.
Working knowledge of EU regulations preferred.
Proficiency with Microsoft office (Word, Excel, Outlook) required.
Ability to interact with internal stakeholders and external customers.

Travel Expectations:

Up to 5% domestic travel.

Physical Demands and Work Environment:

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. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is required to frequently stand, walk, sit; talk or hear; use hands to finger, handle or feel. The employee is required some of the time to reach with hands and arms. The employee is required occasionally to climb or balance; and taste or smell. The employee must frequently lift and/or move up to 25 pounds. There is no special vision requirement for this job. The employee may occasionally work near moving mechanical parts; fumes or airborne particles; toxic or caustic chemicals.

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Refine Your Search

process engineer parenteral jobs

Sr. Process Engineer

Process Engineer

Manufacturing Process Engineer

Process Engineer

Parenteral Process Scientist or Engineer

Engineer - Process

Process Validation Engineer

Scientist / Senior Engineer – Drug Product Process Engineering

Senior Process Engineer

Packaging Engineer III

Technical Development Principal Scientist - Computational Biophysics

Process Engineer

Manufacturing Process Engineer

Senior Human Factors Engineer

Manufacturing Process Engineer

Senior Engineer - Process Optimization & Capital Projects

Development Engineer

Sr Engineer

Sr. Engineer

Cleaning Validation Engineer II

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