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Biotech Companies In Jobs in Indiana (NOW HIRING)

Simtra US LLC

Microbiology Manager

Bloomington, IN · On-site

... and biotech companies to bring their sterile injectable products to market. With facilities in Bloomington, Indiana, US and Halle/Westfalen, Germany, we offer a wide range of delivery systems ...

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Biotech Companies In information

Which biotech jobs are in high demand?

Biotech roles such as research scientists, clinical research associates, and quality assurance specialists are currently in high demand due to ongoing advancements in medical research and product development. Skills in molecular biology, data analysis, and regulatory compliance, along with relevant certifications, enhance employability in this sector.

What jobs come from biotech?

Biotech companies offer a variety of jobs including research scientists, laboratory technicians, quality assurance specialists, regulatory affairs managers, clinical trial coordinators, and manufacturing operators. These roles often require knowledge of biology, chemistry, or related sciences, and may involve working with laboratory equipment, data analysis, or compliance with industry regulations.

Which biotech companies are doing well?

Biotech companies that are currently performing well include those involved in innovative areas such as gene therapy, immunotherapy, and personalized medicine. Leading firms often have strong research pipelines, robust funding, and regulatory approvals for their products, creating opportunities for biotech professionals with skills in molecular biology, clinical research, and regulatory affairs.

What are the key skills and qualifications needed to thrive as a Biotechnology Industry Professional, and why are they important?

To thrive as a professional in a biotechnology company, you generally need a background in life sciences, chemistry, or engineering, often supported by a relevant degree or advanced studies. Familiarity with laboratory techniques, data analysis software, and regulatory compliance systems like GLP, GMP, or FDA guidelines is typical. Strong problem-solving abilities, teamwork, and effective communication skills help individuals excel in cross-functional biotech environments. These competencies enable professionals to drive innovation, ensure product quality, and navigate regulatory landscapes essential for the success of biotech organizations.

What are biotech companies?

Biotech companies are organizations that use biological processes, organisms, or systems to develop products and technologies that improve human life. These companies often focus on areas such as healthcare, agriculture, environmental science, and industrial applications. They may develop new medicines, genetically modified crops, diagnostic tools, or sustainable manufacturing processes. Biotech companies play a vital role in innovation and often collaborate with research institutions and government agencies.

What is the difference between Biotech Companies In vs Biotech Research Associates?

AspectBiotech Companies InBiotech Research Associates
CredentialsBachelor's or Master's in Life SciencesBachelor's or Master's in Life Sciences
Work EnvironmentCorporate labs, R&D departmentsResearch labs, clinical settings
Employer & Industry UsageBiotech firms, pharmaceutical companiesResearch institutions, biotech firms
Common Search & ComparisonYesYes

Biotech Companies In typically refers to employment within biotech firms' corporate environments, focusing on product development and commercialization. Biotech Research Associates usually work in research labs or clinical settings, concentrating on experimental and scientific research. Both roles require similar educational backgrounds but differ in work focus and environment.

What is the best biotech company to work for?

The best biotech company to work for varies based on individual preferences, but companies like Gilead Sciences, Amgen, and Biogen are often recognized for strong research programs, competitive benefits, and positive workplace cultures. Factors such as job role, location, and career development opportunities also influence the best fit for each candidate.

What are some common challenges faced by employees working in biotech companies?

Employees in biotech companies often face challenges such as rapidly evolving technology, tight project deadlines, and strict regulatory compliance requirements. Collaboration across multidisciplinary teams—including scientists, engineers, and regulatory professionals—is crucial, which can sometimes lead to communication hurdles. Additionally, adapting to shifting project priorities and maintaining flexibility in a dynamic environment are important for success. Despite these challenges, the work is rewarding and offers significant opportunities for professional growth and impact.
What are popular job titles related to Biotech Companies In jobs in Indiana? For Biotech Companies In jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Biotech Companies In jobs in Indiana look for? The top searched job categories for Biotech Companies In jobs in Indiana are:
What cities in Indiana are hiring for Biotech Companies In jobs? Cities in Indiana with the most Biotech Companies In job openings:
Biotech Companies In jobs near you

Packaging Validation Associate I - 1st Shift

Simtra BioPharma Solutions

Bloomington, IN • On-site

$14 - $17/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 20 days ago

Job description

Simtra BioPharma Solutions (Simtra) is a world-class Contract Development Manufacturing Organization, partnering with pharmaceutical and biotech companies to bring their sterile injectable products to market. With facilities in Bloomington, Indiana, US and Halle/Westfalen, Germany, we offer a wide range of delivery systems including pre-filled syringes, liquid/lyophilized vials, diluents for reconstitution, powder-filled vials and sterile crystallization.
Our product types include biologics and small molecules, cytotoxics, highly potent compounds, diluents for reconstitution and vaccines - which are all directly injected into patients worldwide. As such, there is a strong emphasis on quality and continuous improvement at Simtra. We hold ourselves to the highest quality and regulatory standards.
While our primary focus is cGMP manufacturing, we offer many support services including formulation and development, lyophilization optimization, global regulatory support and secondary packaging. Our teams are driven to help clients scale, innovate and bring life-changing medicines to patients worldwide.
Why join Team Simtra? Because we:
Make it HAPPEN - We bring a growth mindset to every opportunity, developing new skillsets and exceeding our expectations and those of our customers.
Make it TOGETHER - We work as one, respecting each voice and tapping into our unique strengths across teams-so we can solve problems in new ways.
Make it RIGHT - We hold ourselves to a high standard of excellence, fulfilling our commitments to the customer, their patients, and our team members.
Make it COUNT - We take pride in our day-to-day work, knowing the impact we make - taking on challenges big and small to improve patient health.
This role:
The Packaging Validation Associate I supports all aspects of the packaging process. This includes packaging development, equipment validation and general finishing operations. The position supports Packaging Development including the defining of packaging requirements, materials selection, package design, prototype development, package testing and the development of all related packaging documentation. It also supports Packaging Validation including packaging equipment design, specification development, installation, qualification, vision tuning, validation and operational support. This position reports to the Manager, Packaging Validation.
The responsibilities:
  • Manages multiple projects providing technical support for packaging operations while working in a cross-functional team environment
  • Develops and executes Validation documentation including Process Flow Diagrams, Failure Mode Effect Analysis (FMEAs), Protocols, Final Reports, Standard Operating Procedures (SOPs), etc.
  • Assists Engineering Department on Factory Acceptance Tests (FAT) and User Requirement Specifications (URS)
  • Participates in small project teams, creates timelines, tracks deliverables and communicates status updates to stakeholders.
  • Formulates and recommends validation procedures and technical work in accordance with project and business objectives
  • Participates in client and regulatory audits
  • Selects packaging materials; evaluates packaging components in terms of functionality and machinability; develops Bill of Materials (BOM), Component Specifications and Process Assembly Specifications
  • Acts as Change Control Management (CCM) Owner, Non-Conformance and OCR (Out of Control Report) author
  • Identifies and implements changes to Automated Inspection Machines
  • Reviews and approves Packaging Technical Services documents

Desired qualifications:
  • Bachelor's degree in science or engineering related area is preferred or a minimum of 5 years manufacturing experience with 2 years of leadership experience required.
  • In-depth process knowledge of related manufacturing equipment and process preferred
  • Experienced understanding of cGMPs and other regulatory guidelines applicable to the medical/pharmaceutical industry preferred
  • Ability to review Equipment Manuals including Engineering Equipment Drawings and Electrical Schematic Diagrams.
  • Proficiency in Microsoft Word, Excel, and Outlook and the ability to use enterprise software (examples include: JDE, BPLM, Trackwise, etc.)
  • Manages time effectively and independently within assigned responsibilities
  • Ability to prioritize multiple projects/workflows and manage time efficiently in order to meet established timelines
  • Operates as a self-starter having the ability to complete tasks with minimal direction from manager
  • Exhibits a sense of urgency to meet timelines and key milestones
  • Possesses good leadership skills including ability to lead cross-functional departments in the implementation of new systems and modification of existing ones

Physical / Safety Requirements:
  • Must be able to lift up to 25 lbs.
  • Duties may require overtime work, including nights and weekends
  • Use of hands and fingers to manipulate office equipment is required
  • Position requires sitting/standing for long hours, but may involve walking or standing for periods of time
  • Must wear appropriate Personal Protective Equipment as applicable
  • Must fully understand company safety rules and regulations

In return, you'll be eligible for[1]:
  • Day One Benefits
    • Medical & Dental Coverage
    • Flexible Spending Accounts
    • Life and AD&D Insurance
    • Supplemental Life Insurance
      • Spouse Life Insurance
      • Child Life Insurance
    • 401(k) Retirement Savings Plan with Company Match
    • Time Off Program
      • Paid Holidays
      • Paid Time Off
      • Paid Parental Leave and more
    • Adoption Reimbursement Program
    • Education Assistance Program
    • Employee Assistance Program
    • Community and Volunteer Service Program
    • Employee Ownership Plan
  • Additional Benefits
    • Short and Long-Term Disability Insurance
    • Voluntary Insurance Benefits
      • Vision Coverage
      • Accident
      • Critical Illness
      • Hospital Indemnity Insurance
      • Identity Theft Protection
      • Legal and more
    • Onsite Campus Amenities
      • Workout Facility
      • Cafeteria
      • Credit Union

[1] Current benefit offerings are in effect through 12/31/26
Disclaimer
This job description is intended to provide the minimum knowledge, skills and abilities necessary to perform the job. It may not be inclusive of all the duties and responsibilities of the job. Simtra reserves the right to make modifications based on business requirements.
Equal Employment Opportunity
Simtra is proud to be an equal opportunity employer. Simtra evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.
Data Privacy
To learn more about Simtra's approach to data privacy, please review the Simtra Recruitment Platform Global Privacy Policy: https://simtra.com/privacy-policy/

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