Aequor Jobs in Usa

Title: Quality Engineer – CSV & Digital Systems

Davie, FL

Shift Details: Monday to Friday 8am – 5 pm (40 hours per week)

Assignment Duration: 6 months with possible extension

Convert to Perm: Depending on opens and performance

Core Essential skill sets (must have):

• Recent Master’s graduate Master's degree in Engineering, Computer Science, Life Sciences, or related field.
• Min 3 years experience in pharmaceutical or regulated manufacturing; out of which 2 years in quality organization
• Min 3 years hands-on CSV experience reviewing and approving validation documentation.
• Direct experience supporting manufacturing or utilities systems (not just lab systems).

Medical screening requirements:

Screenings:

1. Basic Bkg
2. 11 Panel drug + Fentanyl
3. Medical Screenings:
4. a) Vision Screen - Near, Far, Color, Depth and Peripheral
5. b) Spirometry & OSHA Respirator Questionnaire

Key Responsibilities:

Computer System Validation (CSV)

• Review and approve CSV lifecycle documents (VMP, URS, FRS, HDS, Risk Assessments, IQ/OQ/PQ, RTM, Summary Reports).
• Ensure risk-based validation approaches aligned with GAMP 5, 21 CFR Part 11, and Data Integrity (ALCOA+) principles.
• Evaluate system changes through change control, assessing GxP impact and validation requirements.
• Support periodic reviews and re-validation activities for existing systems.

Digital Systems & Platforms

• Act as Quality reviewer/approver for systems including:
• o MES / EBR platforms (e.g., Werum PAS-X or similar)
• o Historians (OSIsoft PI or equivalent)
• o Advanced analytics tools (Seeq, used for GxP trending)
• o Empower and other lab systems
• Review configurations related to data acquisition, time stamping, audit trails, access control, and electronic records/signatures.
• Ensure proper segregation between GxP vs non-GxP analytics use cases.

Data Integrity & Compliance:

• Assess and approve data flows, interfaces, and integrations between systems.
• Support regulatory inspections (FDA, EMA) and internal audits related to computerized systems.

Cross-Functional Collaboration

• Partner with Engineering, Automation, MS&T, IT, and Operations to:
• o Enable faster project execution with compliant validation strategies
• o Avoid over-validation while maintaining inspection readiness
• Provide Quality input during project design, FAT/SAT, and commissioning phases.

Required Qualifications:

Education:

• Master's degree in Engineering, Computer Science, Life Sciences, or related field.

Experience:

• 3-5 years experience in pharmaceutical or regulated manufacturing; out of which 2 years in quality organization
• 3+ years hands-on CSV experience reviewing and approving validation documentation.
• Direct experience supporting manufacturing or utilities systems (not just lab systems).

Required Technical Skills

• Strong working knowledge of:
• o CSV lifecycle & GAMP 5
• o 21 CFR Part 11 / Annex 11
• o Data Integrity (ALCOA+)
• Practical experience with:
• o MES / EBR systems
• o Process Historians (PI, etc.)
• o Advanced analytics platforms (Seeq) in a GxP context
• Ability to evaluate risk-based validation for dashboards, reports, and models.
• Familiarity with change control, deviations, and CAPA systems.

Preferred / Nice-to-Have

• Experience with:
• o Werum PAS-X, Seeq, PI Vision, Power BI (for regulated trending)
• o Agile or lean validation approaches
• o Commissioning & Qualification (C&Q) integration with CSV
• Prior involvement in:
• o FDA inspections related to computerized systems
• o Site digitalization or Industry 4.0 initiatives

Key Competencies

• Risk-based decision making with quality and compliance focus
• Strong documentation review and technical writing skills
• Ability to challenge constructively while remaining solution-oriented
• Comfortable working at the intersection of Quality, Engineering, and IT
• Pragmatic mindset: compliant and business-enabling

Job Title: Quality Technician - Quality Control

Location: Pearl River, NY 10965

Duration: 6 Months Contract

Pay rate: $30/hr on w2

Shift: 1st Work Schedule: Monday through Friday, Weekend work possible

3+ years of professional experience considered overqualified, this is an entry level role

Open to candidates willing to relocate at own expense

Possibility of extension

Free parking onsite

Fully onsite

MS and PHD degrees considered overqualified

Role will work in a team lab environment

no heaving lifting

Exposure to and will work with Isopropyl alcohol

- Must have Skills/ Experience:

Bachelors degree science degree (Biochemistry, Chemistry, Biology, Molecular Biology, Immunology and or related disciplines)

Previous lab experience in school or professional role

MS Office

Position Summary:

This position supports daily routine activities in the Quality Control laboratory, while adhering to site work instructions and procedures. This position requires the individual to perform routine cGMP activities as scheduled to support laboratory testing and functions.

Activities to be performed by this role include Environmental Monitoring (EM) of laboratory spaces, Bioburden and EM sample incubation, transfer and reads, results documentation and entry into data management system, maintenance of laboratory supplies and inventory, sample receipt, sample inventory and tracking, and cleaning of GMP lab spaces, Biological Safety Cabinets, and controlled temperature units according to current procedures. Additional activities may be assigned as required.

Key Accountabilities

Performs current lab support activities as described by strictly adhering to SOP, SWI, Federal Regulations, cGMP, training modules (when applicable), *** Pasteur policies and procedures and safety procedures. Performs laboratory support activities as scheduled by laboratory management to meet the needs of the QC Microbiology Lab.

Completes required paperwork and documentation in a cGMP laboratory as per company procedures.

Assist with maintaining safety and compliance of the laboratory work area; Perform cleaning of laboratories, equipment, and ancillary areas as required; Attend/Contribute to scheduled team meetings, department and safety meetings.

Performs peer review of laboratory documentation.

Performs additional activities related to QC laboratory operations when required.

Basic Qualifications:

4 years' science degree (Biochemistry, Chemistry, Biology, Molecular Biology, Immunology and or related disciplines)

Preferred Skills:

Prior hands-on laboratory experience.

Please contact me if you are interested. Thank you.

Thanks & Regards

Mukesh Sharma

Lead Recruiter

O 6

is the premier career resource and networking hub for the Pharmaceutical, Biotechnology, and Medical Device sectors. Our parent company Aequor, a global leader in staffing and consulting with a 28-year legacy, we offer our clients a comprehensive suite of recruitment solutions.

We are seeking a hunter-mentality Account Executive to drive revenue by connecting world-class Life Science employers with our elite candidate network. If you thrive in a consultative sales environment and want to work at the intersection of healthcare innovation and talent acquisition, this is your next career move.

Core Responsibilities

• Revenue Generation: Meet and exceed sales quotas by selling a diversified portfolio: online recruitment advertising, career fair registrations, and traditional staffing placement services.
• Full-Cycle Business Development: Identify, qualify, and prospect high-value Life Science employers (Pharma, Biotech, Med-Device) to build a robust national book of business.
• Consultative Selling: Act as a strategic partner to Talent Acquisition leaders, diagnosing their hiring pain points and tailoring solutions to meet their recruitment goals.
• Pipeline Management: Maintain a high volume of sales activity—including cold calling, networking, and presentations—to ensure a consistent flow of new revenue.
• Account Farming: Grow existing client relationships by identifying upsell opportunities and maximizing staffing service utilization.
• Data Integrity: Utilize our CRM to meticulously track activities, communications, and forecasts, ensuring accurate reporting for the leadership team.

Position Requirements

• Experience: 4+ years of B2B sales experience, specifically in Advertising Sales, Talent Acquisition, or SaaS.
• Industry Knowledge: A background in Life Science recruitment is highly preferred and considered a significant plus.
• Education: Minimum of an Associate’s degree (Business, Marketing, or related field preferred).
• Skills: * Proven track record of building a book of business from scratch.
• Exceptional time management and the ability to prioritize high-value activities.
• Strong "storytelling" ability—you can clearly articulate the value of our platform to HR executives.
• Location: Must be able to work onsite at our Piscataway, NJ headquarters.

Why ?

• The Aequor Advantage: Benefit from the stability and reputation of a global parent company with nearly three decades of industry dominance.
• Uncapped Earning Potential: A competitive base salary supplemented by a commission structure that rewards high performance.
• Industry Impact: Play a pivotal role in helping life-saving companies find the talent they need to change the world.

Job Title: Enterprise AI-Ready Data Architect / Senior Data Engineer

Duration : 6 Months

Location: East Hanover (Onsite: 3days & 2 days remote a week)

Job Description:

The Enterprise AI-Ready Data Architect / Senior Data Engineer is a hybrid role with a focus on enterprise data architecture, AI integration, and hands-on data engineering. You will design and implement AI-ready, analytics-ready data products and semantic layers (including ontologies) that enable scalable enterprise analytics and integration with AI agents and GenAI use cases. You will embed governance-by-design (quality, lineage, contracts, observability) and partner closely with business and technology stakeholders—in pharmaceutical domains.

Key Responsibilities

1) Enterprise Data Architecture (AI-Ready by Design)

• Define and deliver strategic enterprise data architectures that scale and support AI-ready outcomes.

• Design data workflows capturing as-is and to-be states for enterprise modernization.

• Establish architecture patterns for:

• Semantic Context Layer

• Data Warehouses, Data Lakehouses

• Data Catalogs and Data Marketplaces

• Event-driven and metadata-driven architectures

• Distributed data management (Data Mesh, Data Fabric, Domain-Driven Design)

• Streaming data management

2) Data Products, Semantic Products, and Master Data

• Design data products that are AI-ready and reusable across domains and use cases.

• Build and govern semantic models, metrics-first modeling, and ontologies (knowledge graph concepts).

• Deliver Master Data Management (MDM) capabilities and align master/reference data with business needs.

• Support structured and unstructured data management to enable broader AI and analytics capabilities.

3) AI Integration and GenAI Enablement

• Enable contextual intelligence and data enrichment using:

• Contextual retrieval, entity linking, enrichment using LLMs and embeddings

• Vector search, RAG pipelines, and LLM-based enrichment

• Implement graph-based approaches:

• RDF, OWL, and SPARQL querying

• Property graph / knowledge graph modeling for relationships and reasoning

4) Data Engineering Delivery

• Design and implement robust ETL/ELT pipelines and orchestration frameworks.

• Develop high-quality transformations and data modeling using:

• Advanced SQL

• Tools such as dbt, Airflow, Dataiku

• Ensure production-grade engineering practices for performance, reliability, and maintainability across pipelines.

5) Governance and Standards (Embedded)

• Implement open-source data standards across:

• Data contracts

• Data quality

• Data lineage

• Lead metadata-driven governance through metadata management, observability, and policy-aligned design.

Skills and Qualifications

Core Technical Skills

Advanced SQL proficiency

Data platforms and governance tooling experience (one or more):

Snowflake, Databricks, Collibra, Salesforce

ELT/ETL and orchestration:

dbt, Airflow, Dataiku

BI and reporting:

Power BI

Cloud platforms:

AWS, Azure, GCP

Modern architecture and data management:

Data Mesh, Data Fabric, streaming, metadata-driven architecture

Graph and semantic technologies:

Knowledge graphs, property graphs (Neo4J), RDF/OWL, SPARQL, graph query languages

Domain and Modeling Expertise

• Experience with data modeling techniques:

• Conceptual, logical, physical modeling—preferably for the pharmaceutical industry

• Semantic modeling, ontology design, and reusable metric layers

• MDM concepts and implementation approaches

AI and GenAI Enablement Skills

• Familiarity with GenAI technologies for enhancing analysis/reporting and data enrichment

• Experience with embeddings, vector search, RAG patterns, and entity resolution/linking concepts

Nice to Have

• Experience with Palantir platform

Recommended Certifications

• CDMP (DAMA)

• TOGAF

• EDM Council frameworks:

• DCAM, CDMC, Open Knowledge Graph, Data Ethics and Responsible AI

Qualifications

• 10+ years of experience in data architecture, process automation, implementation and large-scale data engineering, ideally in pharmaceutical

• Advanced technical engineering and hands-on experience in data modeling for OLAP, workflow automation, AI/ML integration

• ETL pipeline design and development

• Bachelor’s degree in computer science, information technology, engineering, or data science

• Strong problem-solving skills and attention to detail.

• Excellent communication skills with the ability to work with senior stakeholders to translate business requirements to technical data requirements

Job Title: Scientist II - Bioconjugation and Delivery

Location: South San Francisco, CA 94080 (Fully on-site)

Duration: 04/06/2026 to 04/05/2027

Description

** To support Protein Bioconjugation and Conjugate Characterization efforts within the Protein Sciences organization

** To contribute to the Design, Development, and Optimization of Protein Conjugates through advanced conjugation strategies and analytical characterization techniques

Required Qualifications:

• BS or MS degree in Chemistry, Biochemistry, Chemical Biology, Biophysics, Biology, Biomedical Engineering, or related field
• Previous experience with oligonucleotides and/or antibody oligonucleotide generation
• 1 – 5 years of hands-on laboratory experience in protein sciences, bioconjugation, or related drug discovery research
• Protein bioconjugation using chemical and/or enzymatic conjugation methods
• Protein purification techniques (SEC, HIC, IEX)
• Hands-on experience with FPLC, HPLC, or LCMS
• Analytical characterization using SDS-PAGE, colorimetric assays, and 1D/2D Mass Spectrometry
• Data interpretation, reporting, and scientific presentation

Aequor is partnering with a school district in the Austin, TX area to hire a full-time Board Certified Behavior Analyst (BCBA) for a school-based position. This is a great opportunity to work within a collaborative team while supporting students in an educational setting.

About the Role

• Location: Austin, TX area
• Setting: Public school
• Schedule: Full-time, Monday–Friday
• Hours: 37.5–40 hours per week
• Start Date: ASAP
• Contract: Through the end of the school year (with potential renewal)

Responsibilities

• Provide behavior analytic services to students
• Conduct Functional Behavior Assessments (FBAs)
• Develop and oversee Behavior Intervention Plans (BIPs)
• Collaborate with teachers, administrators, and related service providers
• Support IEP development and implementation
• Provide staff training and behavior support strategies

Qualifications

• Active BCBA certification
• Experience working with children or in school settings preferred

Required Skills

• Strong collaboration and data analysis skills

Preferred Skills

• Experience working with children or in school settings preferred

Pay range and compensation package

If you're looking for a structured school schedule and the opportunity to make a meaningful impact, I'd love to connect. Message me directly or apply here on LinkedIn to learn more.

Job Title: Research Associate III or Senior Research Associate (Stability)

Location: Tucson, AZ 85755 (100% on-site)

Duration: 2 years contract

SKILLS

• Research Associate III - Position requires 4 relevant experience post-college with a Bachelor's degree

• Senior Research Associate - Position requires 6 or more years of relevant experience post-college with a Bachelor's degree or 1 year of experience with a Master's degree

• Ideal candidate will have industry experience, as well as experience with IHC and ISH

• Experience in stability studies is required