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Lab Technician I - Laboratory

Trenton, NJ

$19 - $25.25/hr

Properly capture a visual image of the gel with the use of a SYNGENE UV gel reader * Be able to troubleshoot any gel box or power source errors, as well as any gel reader errors Pyrosequencing

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Which job is best for a 40 year old woman?

The best job for a 40-year-old woman depends on her skills, interests, and experience. Roles such as administrative assistant, customer service representative, or project coordinator often value experience and interpersonal skills and can offer flexible schedules. It is important to consider personal strengths and career goals when choosing a suitable position.

Is Syngene a good company to work for?

Syngene is a contract research organization that offers roles in scientific research, manufacturing, and support functions. Employees generally cite a professional work environment, opportunities for skill development, and competitive benefits, though experiences can vary by department and location.

What is the difference between Syngene vs Research Scientist?

AspectSyngeneResearch Scientist
Required CredentialsBachelor's or Master's in Life Sciences, Chemistry, or related fieldsTypically a Master's or Ph.D. in a scientific discipline
Work EnvironmentContract research organization, laboratory settingAcademic, industrial, or corporate research labs
Employer & Industry UsagePharmaceutical, biotech, and contract research organizationsUniversities, research institutes, pharmaceutical companies
Common Search & ComparisonYesYes

Syngene and Research Scientist roles often overlap in scientific research, but Syngene typically refers to a company specializing in contract research services, while Research Scientist is a job title for individuals conducting research across various organizations. Both require strong scientific credentials, but Syngene roles focus more on applied research within a commercial setting.

What kind of company is Syngene?

Syngene is a contract research organization (CRO) that provides research and development services to the pharmaceutical, biotechnology, and consumer goods industries. Employees in roles at Syngene often work in laboratories, utilizing scientific skills and tools to support client projects across drug discovery, development, and manufacturing processes.

Why is Syngene falling?

If referring to Syngene as a company, its stock price may decline due to factors such as market volatility, financial performance, or industry challenges. For employees or job seekers, a decline in company performance can impact job stability, but specific reasons vary based on economic conditions and company management strategies.

What are the key skills and qualifications needed to thrive as a Syngene research scientist, and why are they important?

To thrive as a research scientist at Syngene, you need a strong background in life sciences, chemistry, or biotechnology, typically supported by a relevant degree (such as M.Sc., Ph.D., or equivalent). Familiarity with laboratory information management systems (LIMS), advanced analytical instruments, and industry-standard protocols is common in this role. Strong analytical thinking, attention to detail, and effective teamwork are valuable soft skills that set exceptional candidates apart. Mastery of these competencies ensures high-quality research outcomes, compliance with safety standards, and successful collaboration in a fast-paced contract research environment.

What are some common challenges faced by scientists working at Syngene, and how can they be addressed?

Scientists at Syngene often work on multidisciplinary projects with tight deadlines and high client expectations, which can present challenges in managing workload and ensuring clear communication across teams. Adapting quickly to new scientific techniques and regulatory requirements is also a common aspect of the role. To address these challenges, Syngene promotes cross-functional collaboration, regular team meetings, and ongoing professional development. Being proactive in seeking feedback and leveraging internal knowledge-sharing platforms can greatly help scientists succeed in this dynamic environment.

What is a Syngene and what do they do?

Syngene is not a job title, but rather the name of a leading global contract research, development, and manufacturing organization (CRDMO) that partners with pharmaceutical, biotechnology, and other industries. Employees at Syngene work in various scientific, technical, and support roles to provide research services in drug discovery, development, and manufacturing. The company’s teams contribute to projects involving chemistry, biology, toxicology, and analytical research, supporting clients worldwide in bringing innovative healthcare solutions to market.
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Syngene jobs near you

Senior Manufacturing Bioprocess Associate (Downstream)

Syngene International Limited

Baltimore, MD • On-site

Full-time

Posted 2 hours ago

Job description

Job Title: Senior Manufacturing Bioprocess Associate (Downstream)
Job Location: Baltimore, USA
Reports To : Supervisor, Manufacturing
Department : Manufacturing
About Syngene: Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply.
At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and SOPs, in letter and spirit.
Mandatory expectation for all roles as per Syngene safety guidelines
  • Overall adherence to safe practices and procedures of oneself and respective teams.
  • Contributing to the development of procedures, practices and systems that ensure safe operations and compliance with the company's integrity & quality standards.
  • Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace.
  • Ensuring safety of self, teams, and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements always in the workplace.
  • Ensure all assigned mandatory training related to data integrity, health, and safety measures are completed on time by all members of the team including self
  • Compliance to Syngene' s quality standards.

Core Purpose of the Role:
The Senior Manufacturing Bioprocess Associate (Downstream) performs complex biologics manufacturing activities with minimal supervision. This role supports upstream or downstream operations including buffer/media preparation, process equipment operation, system setup, and sterilization support.
Role Accountabilities
  • 1. Manufacturing Operations
    • Execute upstream (seed train, bioreactor) or downstream (chromatography, TFF) unit operations in accordance with batch requirements.
    • Prepare and test media or buffer solutions following SOPs and batch instructions, including pH and conductivity adjustments.
    • Operate and maintain glass wash and autoclave systems to ensure proper sterilization and availability of process components.
    • Assist in system setup, tubing configurations, and filter integrity testing.
    • Perform cleaning, sanitization, and line clearance of equipment and cleanroom areas.
    • Execute Master Batch Records (MBR) under cGMP and document all operations clearly using SOPs and batch records.

    3. Quality/Compliance
    • Execute Master Batch Records (MBR) under cGMP, and document in detail through the use of SOPs and MBRs for the processes and manufacturing steps.
    • Ensure strict adherence to cGMP standards, FDA/EMA regulatory requirements, and internal SOPs.
    • Support deviation investigations, root cause analysis, and implementation of effective CAPAs.
    • Adhere to data integrity and robust documentation practices, including completion of batch records and change controls.
    • Ensure cGMP compliance of batch records, logbooks, and cleaning documentation.
    • Contribute to deviation investigations, CAPA development, and quality documentation.
    • Support 24/7 operations as needed, including off-shift or weekend coverage.
    • All other duties as assigned

    4. Process Introduction & Technology Transfer
    • Serve as the manufacturing support for new product introductions (NPI), working closely with MSAT and Process Development.
    • Ensure facility and equipment readiness, documentation preparations (SOPs and Master Batch Records, and personnel training for new processes.
    • Support execution of process performance qualification (PPQ) batches and readiness for commercial launch.

    5. Continuous Improvement & Operational Excellence
    • 5S standards are maintained
    • Propose and implement process improvements.

    The responsibilities listed below represent the core expectations of the role; however, this is not an all-inclusive list. The Senior Manufacturing Bioprocess Associate may be assigned additional duties and responsibilities as business needs evolve.

Syngene Values
All employees will consistently demonstrate alignment with our core values.
  • Excellence
  • Integrity
  • Professionalism

Specific requirements for this role
  • Associate or Bachelor degree in a science related field or equivalent relevant experience required.
  • Independently performs standard tasks of biologics manufacturing experience (upstream or downstream).
  • Working knowledge of GMP documentation, cleanroom behaviour, and aseptic techniques.
  • Experience with new facility startup, equipment commissioning/qualification.
  • Deep understanding of upstream (cell culture/fermentation) and Downstream (purification) unit operations for biologics manufacturing.
  • Prior experience supporting client-sponsored manufacturing or operating in a CDMO environment.
  • Experience with Industry Applications such UNICORN, SAP, TrackWise, Delta V is preferred.

Additional requirements for this role:
In this site-based role your work schedule may be fluid to support a 24/7 manufacturing operation, including weekends, nights, and holidays. Schedule changes may occur based on business needs. During Routine production, the Senior Manufacturing Bioprocess Associate is expected to be on the manufacturing floor at least %75 of the time. The physical/mental demands are representative of those that must be met by an individual to successfully perform the essential functions of the job. The work environment characteristics described here are representative of those an individual would encounter while performing the essential functions of the job.
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The role demands good eye/hand coordination, visual acuity, and proficiency in using keyboards, computers, and phones. Sensory awareness-including the ability to detect and distinguish smells and sounds-is important for safety and quality assurance. Physical competencies such as maintaining a stationary position, moving or traversing the facility, ascending or descending (climbing), reaching, and safely operating hand tools and performing repetitive movements are integral, as is the ability to move or transport required loads.
A commitment to regular and predictable attendance is necessary, as is the flexibility to work irregular hours that often include nights and weekends. The position involves working in environments with extreme temperatures, high noise levels, restricted laboratory access, and exposure to dust, gas, fumes, steam, or chemicals. This multifaceted role supports the organization's operational continuity and ensures safety and efficiency across all aspects of manufacturing leadership. The role may require approximately 5% to 10% of travel and may include international travel basis business needs.
Equal Opportunity Employer: It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodation for qualified individuals with disabilities.

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