Maintain robust documentation and audit-ready processes for deviation management, CAPAs, change ... MUST HAVE * Bachelor's degree in Supply Chain Management, Life Sciences, Biotechnology, or a ...
Maintain robust documentation and audit-ready processes for deviation management, CAPAs, change ... MUST HAVE * Bachelor's degree in Supply Chain Management, Life Sciences, Biotechnology, or a ...
... biotechnology oncology, laboratory services, or precision medicine commercial experience * 5 years ... processes, or strategic account management. * 3 years of experience selling pathology ...
... biotechnology oncology, laboratory services, or precision medicine commercial experience * 5 years ... processes, or strategic account management. * 3 years of experience selling pathology ...
Head of Strategic Planning
Iowa, LA · On-site
Lead development and ongoing management of BridgeBio's long-range strategic plan; translate mission ... Own the annual strategic planning process (framework, cross-functional alignment, resource ...
Head of Strategic Planning
Iowa, LA · On-site
Lead development and ongoing management of BridgeBio's long-range strategic plan; translate mission ... Own the annual strategic planning process (framework, cross-functional alignment, resource ...
Imaging Specialist Manager
New Orleans, LA · On-site +1
... biotech, pharmaceutical or CRO company, having a strong understanding of clinical development ... Good understanding of quality oversight and process improvement * Ability to network and establish ...
Imaging Specialist Manager
New Orleans, LA · On-site +1
... biotech, pharmaceutical or CRO company, having a strong understanding of clinical development ... Good understanding of quality oversight and process improvement * Ability to network and establish ...
Participation in training and development programs while abiding by all industry and corporate ... Strong understanding of hospital decision-making processes, clinical pathways, formulary management ...
Participation in training and development programs while abiding by all industry and corporate ... Strong understanding of hospital decision-making processes, clinical pathways, formulary management ...
Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
Software Engineer Internships
Shreveport, LA · On-site
Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
Software Engineer Internships
Shreveport, LA · On-site
Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
Software Engineer Internships
Baton Rouge, LA · On-site
Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
Software Engineer Internships
Baton Rouge, LA · On-site
Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
Software Engineer Internships
New Orleans, LA · On-site
Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
Software Engineer Internships
New Orleans, LA · On-site
Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
Software Engineer Internships
Kenner, LA · On-site
Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
Software Engineer Internships
Kenner, LA · On-site
Supporting the development of console and embedded software systems * Troubleshooting issues and ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...
Biotech Process Development information
See Louisiana salary details
$15.98 - $17.79
2% of jobs
$17.79 - $19.59
0% of jobs
$19.59 - $21.39
9% of jobs
$22.65 is the 25th percentile. Wages below this are outliers.
$21.39 - $23.19
20% of jobs
The median wage is $24.57 / hr.
$23.19 - $25
25% of jobs
$25 - $26.80
17% of jobs
$27.43 is the 75th percentile. Wages above this are outliers.
$26.80 - $28.60
5% of jobs
$28.60 - $30.40
4% of jobs
$30.40 - $32.21
4% of jobs
$32.21 - $34.01
3% of jobs
$34.01 - $35.81
10% of jobs
$15
$26
$35
How much do biotech process development jobs pay per hour?
What is biotech process development?
What are the key skills and qualifications needed to thrive in biotech process development, and why are they important?
What are some common challenges faced by professionals in biotech process development, and how are they typically addressed?
What is the difference between Biotech Process Development vs Biotech Manufacturing Associate?
| Aspect | Biotech Process Development | Biotech Manufacturing Associate |
|---|---|---|
| Primary Focus | Designing, optimizing, and scaling up bioprocesses for product development | Executing manufacturing processes to produce biopharmaceuticals at scale |
| Work Environment | Laboratories and pilot plant facilities | Production floors and manufacturing plants |
| Required Skills | Process design, lab techniques, troubleshooting | Equipment operation, quality control, adherence to SOPs |
| Typical Credentials | BSc/MSc in Biotechnology, Chemical Engineering, or related fields | BSc in Biotechnology, Biology, or related fields |
While both roles are essential in biotech, Biotech Process Development focuses on creating and optimizing processes during product development, whereas Biotech Manufacturing Associates handle the day-to-day production to ensure consistent product quality at scale.
What are popular job titles related to Biotech Process Development jobs in Louisiana?
For Biotech Process Development jobs in Louisiana, the most frequently searched job titles are:
What job categories do people searching Biotech Process Development jobs in Louisiana look for?
The top searched job categories for Biotech Process Development jobs in Louisiana are:

Director, Sample Logistics, Vaccines R&D
Pearl River, LA • On-site
Other
Posted 7 days ago
Job description
You will be responsible for managing the clinical sample logistics function for Pfizer’s vaccine clinical portfolio, ensuring samples are transported safely, compliantly, and reliably across domestic and international clinical trial networks to the Pearl River, NY biorepository and then distributed to our network of internal and external testing laboratories.
You will lead an end-to-end logistics strategy from study start-up through operations and finally sample disposition. Your responsibilities include leading a large team, improving global logistics capabilities, advancing digital and automation initiatives, and partnering with Vaccines, Quality, Legal, Finance, Compliance, clinical study teams, couriers, and technology vendors.
You will be accountable for maintaining sample integrity, enabling global clinical trial execution, and developing scalable logistics processes to support Pfizer’s vaccine pipeline.
KEY RESPONSIBILITIES- Lead the global sample logistics function--Provide strategic and operational leadership for a team of 40+ colleagues responsible for domestic and international shipment execution, study start-up support, ongoing operations, and clinical sample lifecycle management.
- Shape long-term sample logistics strategy. Develop scalable operating models, governance frameworks, and business continuity plans that support pipeline growth, clinical trial expansion, and evolving global regulatory expectations.
- Protect sample integrity and compliance. Ensure reliable, temperature-controlled movement of clinical biological samples while maintaining adherence to applicable FDA, EMA, IATA, DOT, CDC, trade compliance, GCLP, and Pfizer quality requirements.
- Advance inspection readiness and quality oversight. Maintain robust documentation and audit-ready processes for deviation management, CAPAs, change controls, and training across sample logistics activities.
- Drive vendor governance and external partnership performance. Own courier and technology partner governance, service expectations, escalation pathways, performance metrics, contracts, and continuous improvement initiatives.
- Modernize operations through digital and automation innovation. Lead automation, robotics, dashboarding, track-and-trace, predictive planning, AI-enabled sample management, and performance analytics initiatives that improve visibility, decision-making, compliance, and efficiency.
- Partner across the enterprise. Serve as a Vaccines representative and subject matter expert in cross-functional forums involving clinical assay teams, study management, Quality, Legal, Finance, Trade Compliance, Research Informatics, Project Management, Data Management, and external partners.
- Develop people and culture. Lead workforce planning, talent acquisition, performance management, career development, and succession planning while fostering high morale, collaboration, accountability, continuous learning, and open communication.
- Communicate with executive impact. Present complex logistics data, risk profiles, investment needs, and operational improvement opportunities clearly to senior leaders and cross-functional decision-makers.
- Bachelor’s degree in Supply Chain Management, Life Sciences, Biotechnology, or a related discipline.
- 8+ years of logistics, supply chain, clinical trial operations, central laboratory, or biopharmaceutical experience.
- 5+ years of direct people management experience, including successful leadership of large teams or multi-tiered management structures.
- Experience leading in a regulated environment and making sound judgments to complex operational, quality, compliance, and risk-management decisions.
- Knowledge of global sample logistics, cold-chain management, temperature-controlled shipping, customs requirements, infectious substance transport, and biohazard shipping regulations.
- Proven success building relationships, influencing without direct authority, negotiating with internal and external stakeholders, and leading through matrixed teams.
- Excellent verbal and written communication skills, including the ability to translate complex operational information into clear recommendations for senior leadership.
- Strong change agility, problem-solving skills, and experience managing competing priorities in a fast-paced environment.
- Advanced degree in Supply Chain Management, Life Sciences, Biotechnology, Business Administration, or a related discipline.
- Experience working in a GCLP, GLP, GMP, clinical trial, vaccine, central laboratory, or regulated sample management environment.
- Experience leading automation, robotics, digital tools, dashboards, AI-enabled capabilities, or analytics initiatives in clinical operations, logistics, laboratory, or supply chain settings.
- Experience overseeing external vendors, couriers, technology partners, contracts, service levels, and supplier performance improvement.
- Experience defining and leading complex programs, executing with quality and timeliness, and delivering measurable business impact.
Ability to perform work while sitting or standing and to operate effectively in a complex, highly regulated, and deadline-driven environment.
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTSThis position may require occasional evening or weekend work to support critical business timelines, global shipment needs, or issue escalation.
Occasional travel may be required for Pfizer site visits, courier or CRO interactions, scientific meetings, inspections, or other business needs.
WORK LOCATION ASSIGNMENTOn Premise
COMPENSATION & BENEFITSThe annual base salary for this position ranges from $176,600.00 to $294,300.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 20.0% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.
Relocation support available
Relocation assistance may be available based on business needs and/or eligibility.
Candidates must be authorized to be employed in the U.S. by any employer.
U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.
SUNSHINE ACTPfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.
EEO & Employment EligibilityPfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.
ACCESSIBILITYPfizer endeavors to make www.pfizer.com/careers accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email disabilityrecruitment@pfizer.com . This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.
AI-USE GUIDELINESTo learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers .