Process Development Scientist/Engineer

Singota Solutions

Bloomington (IN)

On-site

USD 75,000 - 95,000

Full time

14 days+

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Benefits offered by this job

Dental insurance

Health insurance

Vision insurance

Health savings account

Life insurance

Paid time off

Tuition reimbursement

401(k)

401(k) matching

Job summary

A leading company in the pharmaceutical manufacturing sector is looking for a Process Development Scientist/Engineer 1. The role involves supporting product development, ensuring compliance with regulatory requirements, and contributing to process improvements. Candidates should possess a degree in a scientific discipline and relevant industry experience. Join us to be part of a diverse team working towards fulfilling business goals.

Qualifications

2+ years’ experience in pharma industry preferred.
4+ years’ experience in pharma industry required with Associates degree.
Operational knowledge of Cytiva/Vanrx SA25 or other robotic filling isolator is a plus.

Responsibilities

Support the Product and Process Development department as a technical transfer liaison.
Identify process improvements and support planning and implementation.
Author, edit, review, and execute procedures and protocols.

Skills

Communication skills

Time management

Organizational skills

Math skills

Chemistry skills

Education

Bachelor's degree in a scientific discipline

Associate's degree in a scientific discipline

Tools

Microsoft Office

ERP systems

Job description

1 month ago Be among the first 25 applicants

JD243
Job Title: Process Development Scientist/Engineer 1
Department: Process Development & Technical Operations
Reports to: Manager, Product & Process Development & Quality Control
Location: Bloomington, IN (Onsite)
Position Type: Full-time, 40 hours/week, Exempt

General Responsibilities:
1. Support the Product and Process Development department as a technical transfer liaison and technical writer on parenteral drug product manufacturing projects.
2. Stays current with bodies of knowledge, identifying best practices, regulatory requirements, industry standards and trends.
3. Share knowledge gained with Singota employees.
4. Identify process improvements and support planning and implementation.
5. Author, edit, review, and execute procedures and protocols.
6. Assist in authoring Batch Records and Specification sheets for Formulation, Filling, Inspection and Finishing.
7. Collaborate in writing and responding to deviations, investigations, and corrective actions.
8. Maintains knowledge of and performs functions in compliance with laws and regulations including
but not limited to Company’s policies and standard operating procedures, FDA and similar regulatory authorities.
9. Positive Attitude and willingness to work as part of a diverse team to achieve overall goals of the company.
10. Comply with quality and safety management systems including requirements for documentation, training, system use, SOPs, processes, and procedures. Ensure procedures are followed and changed if no longer applicable.
11. General support required of a company where everyone is expected to perform multiple tasks both inside and outside their department to meet the needs of the business.
12. Operational knowledge of Cytiva/Vanrx SA25 or other robotic filling isolator is a plus.

Requirements

Skills and Physical Activity Requirements:
1. Able to support the client team in organizing and leading meetings, and driving projects to meet operational deliverables.
2. Proficient with electronic systems, including but not limited to enterprise resource planning (ERP), and Microsoft Office applications, particularly Word, Excel, PowerPoint and Project.
3. Trustworthiness and personal integrity – able to maintain a high degree of confidentiality
4. Strong verbal, listening and written communication skills.
5. Good time management and organizational skills.
6. Positive attitude and good judgment.
7. Customer focused both to internal staff and external clients.
8. Proficient math and chemistry skills required including knowledge of manufacturing methods.

Education Requirements:
1. Bachelor’s degree in a scientific discipline and 2+ years’ experience in pharma industry, formulation and aseptic manufacturing experience preferred
Or
2. Associates degree in a scientific discipline and 4+ years’ experience in a pharma industry, formulation and aseptic manufacturing experience required

Benefits