Bioprocess Automation Engineer Job at Randstad (Bangalore)

New

Sr. Engineer, ARI Engineering Projects

Join Amgen's Mission of Serving Patients. At Amgen, if you feel like you're part...

Location

United States , West Greenwich

Salary:

115494.60 - 156257.40 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

High school diploma / GED and 10 years of Engineering experience OR Associate's degree and 8 years of Engineering experience OR Bachelor's degree and 4 years of Engineering experience OR Master's degree and 2 years of Engineering experience OR Doctorate degree
Degree in Chemical Engineering, Mechanical Engineering, Bioprocess Engineering, or related discipline
Experience supporting GMP biopharmaceutical manufacturing operations
Direct knowledge of upstream and/or downstream process equipment including: Bioreactors, Centrifuges, Chromatography systems, UFDF skids, Single-use systems, CIP/SIP systems
Experience with: Commissioning & Qualification (C&Q), Capital project execution, Lifecycle Management Projects, Process troubleshooting, Operational readiness, Manufacturing support
Knowledge of GMP quality systems including: Change controls, Deviations, CAPAs, Risk assessments, Validation documentation
Experience working with DeltaV and process automation systems preferred
Strong technical problem-solving and communication skills
Ability to lead cross-functional initiatives in a fast-paced manufacturing environment
Experience balancing operational support with project execution and continuous improvement initiatives

Job Responsibility

Provide technical expertise in the design and integration of upstream and downstream process equipment
Lead troubleshooting and technical investigations related to process equipment, automation interactions, and operational performance
Support design, construction, startup, commissioning, and qualification of new manufacturing equipment and facility modifications
Review and approve engineering deliverables
Partner with Capital Project teams and Engineering Technical Authorities (ETA) to ensure alignment with Amgen standards and manufacturing requirements
Support utility tie-ins, operational readiness activities, New Product Introductions and hyper care support following startup
Lead and support commissioning and qualification activities for GMP process systems
Identify and implement engineering-based improvements to optimize equipment reliability, throughput, process robustness, and operational efficiency
Lead root cause analysis and implementation of corrective and preventive actions (CAPAs)
Support predictive maintenance, reliability initiatives, and process performance monitoring

What we offer

Health and welfare plans for staff and eligible dependents
Financial plans with opportunities to save towards retirement or other goals
Work/life balance
Career development opportunities
Competitive employee benefits package including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
Discretionary annual bonus program
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible

Fulltime

Sr. Production Process Engineer

We are looking for a Senior Process Engineer to (i) get our newly commissioned F...

Location

United States , Texas City

Salary:

Not provided

Life Science Talent

Expiration Date

Until further notice

Requirements

You have practical experience (>5 years) in production and process engineering in a plant setting
Hands on experience with industrial reactors- operation, optimization, debottlenecking, troubleshooting
BS in Chemical Engineering, Bioprocess Enginering, or similar
You are collaborative, communicative and can work closely with both our scientific and process engineering teams. You can also collaborate with and help give clear direction to our Automation personnel
You lead by example and can operate independently. Although you will be managing other engineers, this is not a desk job - significant presence in the field is required.

Job Responsibility

Oversee production engineering for TXS-1, Again’s first commercial gas fermentation plant
Manage engineers and technicians
Optimize and debottleneck production processes, particularly gas fermentation and related upstream equipment including media preparation. Downstream processing steps will also require your attention
Ensure safe and smooth operation of all plant equipment
Oversee improvement projects and lead root cause analyses (RCA’s)

What we offer

Health, dental, and vision insurance
401k match
company equity
performance bonus
PTO and sick leave
parental leave
stocked kitchen

Fulltime

Senior Director, R&D Bangalore

The Sr Director, R&D Bangalore is responsible for leading a large R&D team compr...

Location

India , Bangalore

Salary:

Not provided

Danaher Corporation

Expiration Date

Until further notice

Requirements

18–20 years of R&D experience
10+ years in leadership roles, preferably within bioprocessing or life sciences
advanced degree in engineering or related scientific discipline preferred
proven ability to lead global, cross-cultural teams in product development and research
demonstrated success in systems engineering and scientific innovation, driving new product development, lifecycle management, and strategic programs
expertise in structured development processes, including toll-gate reviews, stakeholder alignment, and integration of engineering and scientific principles across business functions
strong capability to anticipate trends, navigate ambiguity, and build technology strategies that leverage AI, software-driven solutions, and advanced analytics for bioprocessing applications
deep understanding of customer needs and scientific challenges, with a track record of translating insights into impactful solutions and building enduring global stakeholder relationships

Job Responsibility

Lead a multidisciplinary R&D organization driving scientific innovation and systems engineering excellence for Bioprocessing applications
Partner with global Cytiva Business Units and senior technical leadership to deliver research, product development, and life cycle programs
Define and implement robust systems engineering practices across complex instrument platforms
Drive architecture decisions, risk management, and system-level verification and validation
Champion scientific rigor in bioprocessing solutions, leveraging emerging technologies in AI, machine learning, advanced sensors, and computational modeling
Collaborate closely with software development teams to embed intelligent algorithms, predictive analytics, and automation into instrument platforms
Identify breakthrough opportunities with Cytiva business units and establish technology strategies for next-generation platforms
Lead a team of scientists, systems engineers, and technical leaders, ensuring high engagement and performance
Attract, develop, and retain top scientific and technical talent
Lead and execute charters for cross Danaher India R&D Board in line with strategic priorities

What we offer

Broad array of comprehensive, competitive benefit programs that add value to our lives
health care program
paid time off

Senior Engineer

At Amgen, if you feel like you’re part of something bigger, it’s because you are...

Location

United States , New Albany

Salary:

123098.00 - 149145.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Master’s degree (or foreign equivalent) in Mechanical Engineering or related field & 2 years of experience in the job offered or in an engineering-related occupation
Position requires 2 years involving the following: 1. Applying engineering and scientific principles to bioprocess design and troubleshooting and investigations of bioprocess commercial production
2. Utilizing knowledge of engineering principles for scale up of unit operations from bench to commercial scale
3. Process Characterization and Technical Transfer to large-scale drug product sites, and Process Validation of bioprocess drug products
4. Quality and regulatory systems including TrackWise, drug substance manufacturing, and process validation
5. Applying problem-solving methodologies including fishbone diagrams and The Five Whys model to root cause analysis investigations
and 6. Identifying and evaluating process parameters and conducting statistical analysis using tools including JMP and Minitab.

Job Responsibility

Support the Technical Transfer of the Amgen product portfolio to Amgen Ohio
The provision of technical operations support for the continuous improvement of device assembly and packaging line capacity and performance, and advisory of technical improvement projects
Ensure communication throughout the Amgen Ohio commercial site and Amgen network with all partners and deliver on technical deliverables
Act as the site technical expert for automated and semi-automated device assembly for FDP and non-combination products
Technical expert for new process and existing device assembly technology
Use technical process knowledge and identify the required expertise to resolve process challenges
Utilize technical expertise in combination product assembly
Lead the Commissioning, Qualification and Validation of process and GMP equipment
Own the site master validation plan for GMP equipment and responsible to the maintenance and execution.

What we offer

stock
retirement
medical
life and disability insurance
eligibility for an annual bonus
Retirement and Savings Plan with generous company contributions
group medical, dental and vision coverage
life and disability insurance
flexible spending accounts
discretionary annual bonus program

Fulltime

Automation Engineer

Location

Germany , Dreieich

Salary:

Not provided

Danaher Corporation

Expiration Date

Until further notice

Requirements

MSc or similar education in the automation/software area
Overall experience of a few years in automation design and from development of SCADA/HMI controlled bioprocess systems
Experience from investigation, process improvements, line activities
Development and Implementation experience with automation technologies subjected to project needs that include: PLC programming, for example using Rockwell/Allen-Bradley (Rockwell Studio5000), Siemens TIA Portal, Codesys or similar and Configuration of automation software
An understanding of the automation development process including tasks such as establishing requirements specifications and writing technical reports and documentation following standard methodology

Job Responsibility

Providing expertise and resources for specification, design and implementation work for automation software configurations
Expertise and resources for integration and build of automation software configuration releases and preparation of software configurations as a deliverable
Maintenance and development of procedures/processes that control the development and testing of automation software configurations
Design and implementation of user interfaces for automation software configurations
Design and implementation of algorithms and functions in automation software configurations according to technical specification

What we offer

Being part of a state-of the art working field and shaping the way of future medicines
Development opportunities at Cytiva and within the Danaher Group
International corporate environment in a rapidly growing industry
Attractive salary and bonus system

Fulltime

Sr Manufacturing Associate, Downstream

Be the driving force behind seamless logistics with our client where precision a...

Location

United States , Bristol

Salary:

Not provided

Proclinical

Expiration Date

Until further notice

Requirements

Bachelor's degree in chemistry, biology or engineering
A minimum of 6+ years' experience in a GMP pharmaceutical environment
Experience in normal flow filtrations and tangential flow filtrations (UF/DF)
Experience with optimization of bioprocesses
Direct hands-on experience with preparative chromatography systems (AKTA Pilot, AKTA Ready, AKTA Explorer, etc.), and manual or automated TFF skids
Experience with cGMP manufacturing operations and GxP principles
Understanding and application of cGMP requirements

Job Responsibility

Works in GMP environment and ensures regulatory compliance
Performs Manufacturing activities including: Performs a variety of complex tasks in accordance with cGMP, cGDP, SOPs, and Batch Records
Batch Documentation/Record Generation
Materials sampling, staging, dispensing, and return
Equipment and Room set-up, operation, and cleaning
Use of appropriate personal safety equipment and engineering controls
In-process inspection and sampling
Support investigational and quality systems activities
Assist maintenance in the performance of preventative maintenance activities, troubleshooting and repair of equipment
Participate in continuous improvement activities

Fulltime

New

Cafe Associate

At Sam's Club, we offer competitive pay as well as performance-based bonus award...

Location

United States , Flint

Salary:

17.00 - 25.00 USD / Hour

Walmart

Expiration Date

Until further notice

Requirements

18 years of age or older
Successfully complete all job required trainings and assessments within a prescribed time period

Job Responsibility

Be a Team Member: Maintains up-to date knowledge of product specifications related to prepared food merchandise
collaborating with cross functional teams and helping educate other associates on tools, tasks and resources
communicating effectively with the members of the team
and being flexible to the needs of the business to work in other areas
Be an Expert: Prepares food according to item specifications
understanding and planning the future productions and mass productions
preparing for seasonality
adhering to food safety standards, sanitation guidelines, cold chain compliance, inventory management
operating, maintaining, and sanitizing equipment
and demonstrating an understanding of product and layout execution

What we offer

Medical, vision and dental coverage
401(k)
stock purchase
company-paid life insurance
PTO
parental leave
family care leave
bereavement
jury duty
voting

Fulltime

New

Buyer - Procurement

JD - Buyer - Procurement Role Description Procure the parts from supplier as aga...

Location

India , Hosur

Salary:

Not provided

Randstad

Expiration Date

July 28, 2026

Requirements

7

Job Responsibility

Procure the parts from supplier as against MRP schedule / CBT(EKAN) trigger (EPO / VOR / IB / Service level)
Make necessary follow up with critical supplier ,if necessary visit the supplier and ensure the supplies
Measure and monitor delivery performance of suppliers and receive Action plan for delivery failures
Revisit and Correct the material master for MRP schedule
Co-ordinate with PARTS/SERVICE/QAD/CP for ECO/ECR changes
Co-ordinate with supplier and internal team for logistics management (Vehicle / Returnable)
Co-ordinate with plant team to transfer the premium price / VOR / No po parts from plant as against spares requirement
Control the inventory as per norms
Co-ordinate with CP team to resolve SOB/ PO / Commercial related issue
Adhere and monitor DWM

Select Country

Bioprocess Automation Engineer

Requirements

Nice to have

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