Upstream/Downstream Bioprocess Specialist

at  Thermo Fisher Scientific

Brisbane, Queensland, Australia -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate17 Aug, 2024Not Specified17 May, 2024N/AExcel,Downstream Processing,Microsoft Teams,Cell Culture,Demand Planning,Color,Communication Skills,Chemistry,Powerpoint,BiologyNoNo
Add to Wishlist Apply All Jobs
Required Visa Status:
CitizenGC
US CitizenStudent Visa
H1BCPT
OPTH4 Spouse of H1B
GC Green Card
Employment Type:
Full TimePart Time
PermanentIndependent - 1099
Contract – W2C2H Independent
C2H W2Contract – Corp 2 Corp
Contract to Hire – Corp 2 Corp

Description:

ABOUT US

Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $44 billion. Our Mission is to enable our customers to make the world Healthier, cleaner and Safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, improving patient diagnostics and therapies or increasing efficiency in their laboratories, we are here to support them. Our team of more than 125,000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD. For more information, please visit www.thermofisher.com.
The Brisbane Drug Substance Division is one of the five divisions that make up the Pharma Services Group. At the Brisbane site we specialize in GMP clinical and commercial manufacturing of large molecule biologics including for clinical Phase I, II, and III, applying powerful single use bioreactors and biologics technologies. This allows us to serve the needs of Small/Emerging, Mid-Sized, and Large Pharma sectors globally. The network of Patheon’s drug substance manufacturing sites include St. Louis, USA, Groningen, Netherlands and Brisbane, Australia.
The Upstream/Downstream Bioprocess Specialist reports to the Operations Technical Support Manager of the Pharma Service Group (PSG) and the role is based in Brisbane.

SKILLS AND EXPERIENCE:

  • Must have at least 2+ yrs’ cGMP experience and technical expertise in Cell Culture, Harvest Operations, or Downstream Processing.
  • Have excellent written & verbal communication skills.
  • Ability to work unsupervised, under pressure on multiple tasks and manage priorities independently.
  • Possess strong organizational and planning skills and a commitment to excellence.
  • Preferred to be educated to minimum Degree level in Biology, Chemistry or related field.
  • Sufficient knowledge of Microsoft packages i.e. Word, Excel, PowerPoint, Microsoft Teams.
  • Use of SFLMS, eDMS, Trackwise, SAP.
    We offer competitive compensation and benefits packages, along with opportunities for professional growth and development. If you are a motivated individual with a passion for demand planning and inventory management, we invite you to apply for this exciting opportunity. Watch as our colleagues explain 5 reasons to work with us.
    Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Responsibilities:

  • Works safely in accordance with EHS guidelines and adhere to Patheon cGMP Quality Management System requirements.
  • Becomes subject matter expert (SME), remains trained and qualified in area of expertise, and displays initiative in personal development opportunities to further enhance skills and expertise relevant to the position.
  • Provide SME troubleshooting/oversight and support execution of the batch as needed to deliver the site key performance indicators of Right First Time and On Time Delivery.
  • Builds partnerships and works collaboratively with the Operations Managers in mentoring Operations staffs with a focus on building talent depth and demonstrating positive behaviors as per 4i values.
  • Support operational production and facility maintenance planning as well as the transfer of new technologies/procedures/equipment to Operations to address production demands as per S&OP and MPS.
  • Review manufacturing batch records, standard operating procedures, logbooks, or validation protocols required for Phase III projects as per ICH guidelines.
  • Assists Operations group with deviation investigation and determination/implementation of preventative/corrective actions.
  • Ensure audit readiness within Operations by identifying and addressing gaps as well as preparing story boards and provide SME input during audit.
  • Devises PPI initiatives to drive continuous improvement in Operations.


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Biology chemistry or related field

Proficient

1

Brisbane QLD, Australia