Process Associate Job at InfoMate (Colombo)

Voice Process Associate

BPS - Voice Process Associate role requiring customer service and customer handl...

Location

India , Noida

Salary:

Not provided

Sopra Steria

Expiration Date

Until further notice

Requirements

1-2 years experience
BPS Customer Service/Customer Handling experience
Utilities experience preferred
Excellent communication skills (spoken and written)
Excellent computer proficiency
Comfortable with 24/7 working environment
Comfortable with Flexible-offs
Graduates only - Commerce background

Job Responsibility

Customer service
Customer handling
Voice process operations

What we offer

Inclusive and respectful work environment
Commitment to fighting discrimination
Open to people with disabilities

Fulltime

Data Processing Associate

Are you tech-savvy, detail-oriented, and ready to dive into the world of AI? App...

Location

Philippines , Imus & Bacoor, Cavite

Salary:

Not provided

Appen

Expiration Date

Until further notice

Requirements

Proficient in computer navigation and office software
Above-average communication skills
Experience in customer service (BPO) or data annotation is an advantage
A college degree is preferred, may consider high school graduates along with relevant skills & work experience
Amenable to work on shifting schedule
Must be willing to work on-site in our office located at Imus & Bacoor, Cavite

Job Responsibility

Learn requirements and skills for specific task, able to do the task according to guidelines
Practice to improve annotation skills until the task can be done correctly and efficiently
Annotate and label data with high precision
Review and correct annotations to ensure data quality
Start task officially after practice period, complete the assigned workload every day

Process Validation Associate

This position reports to the Process Validation Manager and is responsible for m...

Location

Ireland , Cork

Salary:

Not provided

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

Bachelor of Arts/Sciences (BA/BS) degree, or higher, in a technical discipline (physical, engineering, chemical or biological sciences) is required
8+ years experience in a cGMP regulated manufacturing environment, with exhibited knowledge or proficiency in process validation, process sciences and change control
Organizational and management skills to participate in multi-discipline project groups
Ability to communicate with, present data to, and defend approaches in front of variable hierarchical audiences, scientific disciplines and health authority reviewers/inspectorate
Ability to comprehend scientific/technical information related to equipment, processes, and regulatory expectations
Understanding and demonstrated knowledge of regulatory requirements, guidelines, and recommendations for process validation expectations
Proficiency with technical writing expected
Proficiency with standard office software applications, including MS Word, MS Excel, MS Project, MS Power Point

Job Responsibility

Perform process validation activities related to BioMarin’s drug substance and drug products, through defined clinical and commercial stages
Execute (protocol generation, execution, and final package preparation) process validation activities related to the implementation of process changes and new processes
Assist with preparation of regulatory filings, with answering questions from regulatory agencies, and with presentations of materials during regulatory inspections/partner audits
Development and implementation of SOPs/Guideline documents with systemic procedural improvements
Determine methods and procedures on new assignments with supervision and in accordance with developed practices and procedures
May participate on sub-teams
Gain/maintain knowledge of industry standards and regulatory requirements for products developed and manufactured by BioMarin, validation techniques/approaches and systems utilized at BioMarin
Participate in multi-departmental meetings & project teams
Identifies and assists with implementation of improvements to Process Validation systems (department level impact)
Generation of process validation master plans, core validation master plans and additional supporting documentation

Fulltime

Sales Processing Associate

This role has been designed as ‘Hybrid’ with an expectation that you will work o...

Location

India , Bangalore

Salary:

Not provided

Hewlett Packard Enterprise

Expiration Date

Until further notice

Requirements

High school or equivalent secondary education certification required
Bachelor's degree preferred
Typically 4 - 6 years experience
High-level administrative and overall documentation and information management skills
Proficient in multiple word processing, spreadsheet, and presentation software packages
Expert user of electronic sales documentation, order management, and bid and quote systems and tools
Complete understanding of basic and advanced order processes, systems configurations and documentation requirements
Strong written and verbal communication skills
mastery in English and local language
Ability to effectively communicate issues and negotiate resolution with local and group management

Job Responsibility

Provides overall support for sales processing activities for an assigned or multiple business areas or groups
Demonstrates comprehensive knowledge and mastery in multiple sales processing areas, including: pricing and creating quotes for moderately- to highly-complex deals
registering information and producing documentation
order execution, billing and invoice production
configuration of order systems according to process standards and with occasional customization
Reviews and provides oversight of all sales processing documentation and systems, including data entry and completion
works with stakeholders to identify areas for process improvement and propose changes to increase quality awareness and culture in the organization
Develops customized data collection forms, methods and reports in response to business requests and in accordance with sales processing systems and standards
Provides guidance to less-experienced staff members

What we offer

Health & Wellbeing
Personal & Professional Development
Unconditional Inclusion

Fulltime

Specialist Process Associate

Ensure daily workload is completed in a timely manner while adhering to process ...

Location

India , Noida

Salary:

Not provided

Sopra Steria

Expiration Date

Until further notice

Requirements

Proven track record auditing/vetting documentation accurately
Well Organised and should be able to multitask
Meet deadlines within fast paced environment
Self-motivated even when undertaking repetitive tasks
Proven ability to build relationships with internal or external parties with excellent telephonic and email communication skills
Process driven and keen to ensure efficiencies are achieved
Excellent problem solving skills and able to use own initiative

Job Responsibility

Ensure daily workload (as provided by the Team Leader/SME) is completed in a timely manner
Adhere to the process defined by the clients to conduct compliance checks / audits ensuring KPI’s are met
Ensure effective & timely communication is maintained with stakeholders (written and verbal)
Build and maintain relationships with stakeholders ensuring they understand the process, resolve their queries within the contractual requirements
Answer calls or make outbound calls to the stakeholders for immediate resolutions
Attend emails (mailbox) ensuring all queries are responded to within the agreed SLA
Be up to date with process updates on compliance requirements and processes
Be efficient in day to day working
Report accurate data on real time basis
Encouraging team camaraderie

Sr. Associate Manufacturing Production Process Owner

In this vital role you will partner with cross-functional teams—including Engine...

Location

United States , Thousand Oaks

Salary:

92002.00 - 108605.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

High school/GED + 4 years Manufacturing support experience
Associate’s + 2 years Manufacturing support experience
Bachelor’s + 6 months Manufacturing support experience
Master's
Advanced degree (Master’s or Ph.D.) in Engineering, Biotechnology, or related field
Experience in aseptic Drug Product or biologics manufacturing
Knowledge of process validation, deviation management, and change control
Strong analytical and problem-solving skills with experience using data visualization tools (Spotfire, JMP, Excel)
Excellent written and verbal communication skills and ability to collaborate across functions

Job Responsibility

Initiate, revise, and approve controlled manufacturing documents within Amgen’s electronic document management system (CDOCs)
Serve as document author, owner, reviewer, or data verifier, ensuring accuracy and compliance with current GMP and Amgen standards
Maintain documentation to accurately reflect operational practices and regulatory requirements
Support implementation of new processes, equipment, and major initiatives within Drug Product operations
Collaborate with Capital, Engineering, Process Development, Quality, and other functions to define requirements and achieve operational readiness
Assist in developing and implementing SOPs, batch records, training, validation, and automation configurations
Analyze manufacturing data and performance metrics to identify trends, deviations, and opportunities for improvement
Develop and implement data-driven solutions to improve yield, reliability, and compliance
Support data monitoring using analytical tools such as Enterprise Data Lake and Spotfire, ensuring configuration alignment with process design and GMP requirements
Support timely investigation and resolution of manufacturing deviations

What we offer

A comprehensive 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
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible

Fulltime

Operations Associate

We are seeking a detail-orientated and highly organised operations associate to ...

Location

India

Salary:

Not provided

Hikinex

Expiration Date

Until further notice

Requirements

Bachelor’s degree in business administration, management, or a related field
Strong analytical and problem-solving skills
Excellent English communication skills and interpersonal skills
Ability to work independently and as part of a team
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)
Willingness to learn and adapt in a fast-paced environment
Previous internship or work experience in a related field is a plus

Job Responsibility

Assist in identifying opportunities for process optimisation and efficiency improvements across different departments
Analyse current workflows and recommend enhancements to streamline operations
Implement best practices and innovative solutions to improve productivity
Support and manage cross-functional projects, ensuring timely and successful completion
Coordinate with various teams to gather requirements, set objectives, and track progress
Deliver project reports and updates to senior management
Conduct data analysis and generate reports to support decision-making processes and strategic initiatives
Utilise analytical tools to interpret data and provide actionable insights
Assist in developing performance metrics and KPIs to monitor departmental success
Participate in training sessions, workshops, and continuous learning opportunities to enhance your skills and knowledge

Fulltime

Manufacturing associate

This is a contract role: ***Shift schedule rotating 12-hour night shift from 6PM...

Location

United States , Novato

Salary:

15.00 - 30.00 USD / Hour

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

Strong communication skills—verbal and written
Ability to work in a team environment which includes good conflict resolution and collaboration
Displays good initiative to identify areas for improvement and implement solutions
Bachelor’s degree in science related area or engineering
Associate’s degree in science related area or Biotech certificate with 2+ years of experience in a biotech manufacturing environment or other regulated industry

Job Responsibility

Understanding of process theory and equipment operation
Ability to learn biopharmaceutical manufacturing processes including mammalian cell culture, depth filtration, tangential flow filtration, column chromatography, centrifugation, protein purification, and formulation of bulk drug substance
Support initiatives for process optimization
Identify and elevate processing issues and support solutions
Gain experience with automation systems (LIMS, MES, PI, etc.)
Provide feedback and/or suggested changes to operational procedures
Assist in the incorporation of new technologies, practices, and standards into procedures
Capable of writing and reviewing process documents
Understanding of cGMPs as related to Commercial Operations
Ability to utilize Quality systems (Deviations, CAPAs, Change Requests, Action/Alert Reports, etc.)

What we offer

discretionary annual bonus
discretionary stock-based long-term incentives
paid time off
company-sponsored medical, dental, vision, and life insurance plans

Fulltime

Process Associate

InfoMate

Location:
Sri Lanka , Colombo

Category:
Finance

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
February 19, 2026

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Job Posted:
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