Bioprocess Automation Engineer Job at Randstad (Bangalore)

Senior Bioprocess Engineer

Location

United Kingdom , Bath

Salary:

40000.00 - 45000.00 GBP / Year

SRG

Expiration Date

Until further notice

Requirements

3-8 years' experience in bioprocessing, bioreactors or related fields
Strong experimental and problem-solving skills
Experience scaling processes from lab to pilot/production
Practical, organised and collaborative approach
Comfortable working in a fast-paced, innovative environment

Job Responsibility

Develop and optimise bioprocess and bioreactor designs
Support scale-up from lab to pilot/manufacturing
Collaborate across biology, engineering and materials teams
Plan and execute experimental work and system testing
Contribute to automation, data capture and process control
Ensure compliance with quality and safety standards

What we offer

Work on cutting-edge biotechnology
Join a collaborative and growing team
Opportunity to shape new processes and technologies

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

Senior Director Research & Development

The Single-Use Technologies Division (SUD) is a global leader in the design and ...

Location

United States , Plainville

Salary:

212000.00 - 317000.00 USD / Year

myGwork - LGBTQ+ Business Community

Expiration Date

Until further notice

Requirements

Bachelor's degree in engineering, physical sciences, or chemistry required
Master's degree or Ph.D. preferred
10+ years of progressive R&D leadership experience, preferably within bioprocessing, bioproduction, or regulated medical device environments
Demonstrated success leading global, multi-site teams and delivering complex products from concept through commercialization
Strong background in bioprocess systems and equipment
experience with single-use technologies strongly preferred
Experience with digital and data-enabled systems (automation, control systems, MES, ERP, historians, analytics) preferred
Ability to influence across functions and operate effectively in a matrixed, fast-paced environment
Ability to travel up to 25% domestically and internationally

Job Responsibility

Serve as an integral member of the SUD leadership team, representing R&D in strategic planning (STRAP), portfolio prioritization, and Annual Operating Plan (AOP) processes
Own and execute the global R&D and product development strategy aligned with the business and market needs
Partner closely with Product Management, Market Development, Manufacturing Engineering, Operations, Quality, and Commercial teams to drive end-to-end lifecycle execution
Engage directly with customers and commercial teams on complex technical programs
Partner with the Bioproduction Group Innovation team, other business groups, and the Corporate Innovation Council to develop next-generation products, platforms, and differentiated intellectual property
Drive technology collaboration across divisions and business units to accelerate innovation and leverage enterprise capabilities
Translate customer and market requirements into differentiated products that meet cost, quality, performance, regulatory, and time-to-market expectations
Lead the advancement of digitalization, automation, and data-enabled technologies within single-use and bioprocessing systems
Champion all aspects of regulated product development, ensuring compliance with design control and quality system requirements
Serve as process owner for New Product Introduction (NPI), Engineer-to-Order (ETO/customization), and product improvement processes

What we offer

A choice of national medical and dental plans, and a national vision plan, including health incentive programs
Employee assistance and family support programs, including commuter benefits and tuition reimbursement
At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount
Variable annual bonus based on company, team, and/or individual performance results

Fulltime

Senior Systems Specialist - Controls Engineering Automation

The Senior Systems Specialist - Controls Engineering is responsible for independ...

Location

India , Bangalore

Salary:

Not provided

Danaher Corporation

Expiration Date

Until further notice

Requirements

Bachelor's degree in Electrical, Electronics, or Instrumentation & Controls Engineering required
A minimum of 8 years of industrial experience in the design and development of industrial automation and control software, including participation in the complete software development lifecycle
Experienced in designing Automation HMI/SCADA solutions, as well as diagnosing and programming programmable logic controllers (PLCs) on at least two platforms such as Aveva System Platform, Rockwell Automation FactoryTalk, DeltaV, Siemens, or similar
Strong experience with hardware interfaces, communication protocols, and PID control loops
Familiarity with Engineering Change Orders (ECO) & Engineering Change Requests (ECR), comprehensive knowledge of PLM tools such as MAGIC, ALM, Azure DevOps, Jira, or equivalent, and practical expertise in defect management, software verification, and testing

Job Responsibility

Oversee and actively contribute to all phases of the automation software development lifecycle, including conceptual design, detailed engineering, simulation/modeling, verification, and validation, ensuring alignment with project objectives and compliance requirements
Support the design, development, and lifecycle management of bioprocessing systems, aiding in the delivery of project milestones and advancing continuous improvement efforts
Lead and implement change management processes, including Engineering Change Requests (ECR) and Engineering Change Orders (ECO), in accordance with established quality and regulatory standards
Identify, assess, and resolve technical challenges, delivering effective solutions and promoting ongoing process enhancements
Provide technical leadership and mentorship to new team members, fostering a collaborative and high-performing work environment

What we offer

health care program
paid time off

Fulltime

Process Development Sr Associate

Support the development, characterization and scale up of cell culture and prote...

Location

United States , Thousand Oaks

Salary:

96605.00 - 119055.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Master's Degree in Biotechnology, Bioengineering, Microbiology or related field and completion of a university-level course, research project, internship, thesis, or one year of experience in the following: Cell culture principles, cell metabolism profiles, protein chromatography, filtration and UF/DF operations to perform small scale bioprocess experiments that encompass both upstream (cell culture) and downstream (purification) operations
Experience with mammalian cell culture to maintain and scale up cell culture in shake flasks, culture bags and bench top bioreactors
Experience with purification operations to run bench-top chromatography columns to generate purified antibody product
Identify and solve problems by applying scientific and engineering principles
Design of experiments and statistical analysis of data and programming in JMP, R, or Python environments
Experience with automation efforts to enable high throughput technologies for accelerated process development

Job Responsibility

Support the development, characterization and scale up of cell culture and protein purification operations to enable commercial manufacturing advancement by conducting experiments, analyzing data, and documenting results
Work closely with senior scientists and engineers to implement process improvements
Support development of early phase cell culture, recovery and purification processes for Amgen's large molecule expansion through production bioreactor, harvest, clarification, chromatography, and/or filtration technologies as well as completing virus clearance studies
Identify, develop and implement solutions to practical problems through application of fundamental scientific and engineering principles

What we offer

stock
retirement
medical insurance
life insurance
disability insurance
eligibility for an annual bonus
health and welfare plans
financial plans with opportunities to save towards retirement or other goals
work/life balance
career development opportunities

Fulltime

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 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

Select Country

Bioprocess Automation Engineer

Requirements

Nice to have

Looking for more opportunities?